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Clinical trial updates
Drug and device trials that companies register on ClinicalTrials.gov: newly completed phase 3 studies, changes of status and the dates a study is due to finish.
About this data
- What it is
- ClinicalTrials.gov is the US registry of clinical studies. Drug and device makers register their trials there and update the record as each study moves on. We list the studies that companies sponsor, and match the sponsor to a public company when the name lines up. The page opens on Phase 3 studies marked completed, the late-stage trials that come before a request for approval. Change View to see the changes of status we have noticed, or every recent update.
- Who files it
- The sponsor of the study, in its record on ClinicalTrials.gov. The registry is run by the US National Library of Medicine and does not check what sponsors report.
- How current
- We check the registry every day. Sponsors update records on their own schedule, from the same week to months later, so a change can appear in the registry well after it happened.
- Terms
- ClinicalTrials.govClinicalTrials.gov is the US government's registry of clinical studies, run by the National Library of Medicine. Sponsors register a study before it starts and update the record as it goes. The registry does not check what a sponsor reports.Phase 3The late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages.statusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time).completedThe sponsor has marked the study as finished. It says nothing about whether the treatment worked: results, if any, are reported separately and often later.status changesOur history of status changes starts the day we first stored each study, so a change made before that is not shown. The date is when we noticed the change, which can be later than when the sponsor made it.primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update.company matchWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private.
- Worth knowing
- A completed study is not a result: the registry says the study ended, not whether the treatment worked. Status changes start on the day we first stored each study, so earlier changes are not shown. Dates are the sponsor's own, and an estimated date can pass without an update. We match sponsors to companies automatically, with a hand-checked list for the large drugmakers, so a study with no ticker may still belong to a public company. This is information about studies, not a forecast of what they will show or of a stock's price.
- Not to be confused with
- FDA approvals and clearances: what the FDA decided, not what a sponsor reports about a study.
All of this comes from ClinicalTrials.gov, the US registry of clinical studies. We are not affiliated with it.
Source and freshness · Information, not investment advice (disclaimer).
Studies updated per day, last 30 days
All industry-sponsored studies Sponsor matched to a public company
By the day the sponsor last updated the study's record. A study updated twice counts once, on its latest day.
Latest clinical trial updates
Showing: ticker IART · All recent updates
Studies by the date their record was last updated.
| Updated | Study | SponsorWe match the sponsor's name to a public company automatically, and by hand for the large drugmakers. A subsidiary or a differently spelled name can be missed, so a study with no ticker does not mean the sponsor is private. | PhaseThe late stage of testing, usually with hundreds or thousands of people, to confirm that a treatment works and to find side effects. A study marked Phase 2/3 covers both stages. | StatusThe registry's own word for where a study stands: not yet recruiting, recruiting, active but not recruiting, completed, terminated (stopped early), withdrawn (never started), suspended, or unknown (the sponsor has not confirmed the record for a long time). | Enrolled | Primary completionThe date the last participant is examined for the main question the study asks. The study can run on after it, for follow-up. Sponsors enter the date and revise it, and an estimated date can pass without an update. | Source |
|---|---|---|---|---|---|---|---|
| Sep 21, 2026 | Tissue Quality of Integra vs. BTM Treated Burns NCT06760611 · Burn Injury, Burn Scar | IART Integra LifeSciences Corporation | — | Withdrawn | 0 | Sep 30, 2025 | Registry ↗ |
| Sep 4, 2026 | Urinary Bladder Matrix (UBM) Registry NCT07805798 · Tissue Repair, Soft Tissue Reconstruction Urinary Bladder Matrix (UBM) Products | IART Integra LifeSciences Corporation | — | Not yet recruiting | 300 | Aug 31, 2029 | Registry ↗ |
| Jul 27, 2026 | A Modified Platform Trial of Multiple CAMPs for the Management of Diabetic Foot Ulcers and Venous L… NCT06453187 · Diabetic Foot Ulcer, Venous Leg Ulcer Urinary Bladder Matrix (UBM) sheet device for Venous Leg Ul… | IART Integra LifeSciences Corporation | Not applicable | Enrolling by invitation | 350 | Dec 31, 2026 | Registry ↗ |
| Jul 7, 2026 | AERA Pediatrics Registry NCT07071298 · Dysfunction of Eustachian Tube | IART Integra LifeSciences Corporation | — | Recruiting | 300 | Oct 2030 | Registry ↗ |
| Mar 5, 2026 | MicroMatrix® Flex in Tunneling Wounds NCT06629506 · Pressure Injury, Venous Ulcer MicroMatrix® Flex, MicroMatrix® UBM Particulate | IART Integra LifeSciences Corporation | Not applicable | Completed | 25 | Aug 31, 2025 | Registry ↗ |
| Feb 27, 2026 | Post Market Clinical Follow-up of CODMAN CERTAS Programmable Valve NCT05397106 · Hydrocephalus, Hydrocephalus in Children CODMAN CERTAS Plus Programmable Valve | IART Integra LifeSciences Corporation | — | Active, not recruiting | 160 | Jan 24, 2029 | Registry ↗ |
| Feb 6, 2026 | The MIRROR Registry: Minimally Invasive IntRaceRebral HemORrhage Evacuation NCT04494295 · Supratentorial Hemorrhage Aurora Surgiscope System | IART Integra LifeSciences Corporation | — | Recruiting | 500 | Oct 15, 2028 | Registry ↗ |
| Jan 28, 2026 | External Ventricular Drainage Post-Market Clinical Follow-up Registry NCT05652296 · Cerebrospinal; Disorder External Ventricular Drainage (EVD) | IART Integra LifeSciences Corporation | — | Completed | 120 | Dec 16, 2024 | Registry ↗ |
| Aug 15, 2025 | The Purpose of This Study is to Determine Whether CerebroFlo™ EVD Catheter is Effective During the… NCT05113381 · Intraventricular Hemorrhage, Subarachnoid Hemorrhage CerebroFlo™ EVD Catheter | IART Integra LifeSciences Corporation | Not applicable | Completed | 105 | Jul 31, 2025 | Registry ↗ |
| May 20, 2025 | T-GENVIH-003 LTFU (Long Term Follow Up) Study NCT06034652 · Hernia, Hernia, Ventral Integra® Gentrix® Surgical Matrix | IART Integra LifeSciences Corporation | — | Completed | 8 | Jan 19, 2024 | Registry ↗ |
| Apr 6, 2025 | Suturable DuraGen™ PMCF Study NCT04923867 · Cerebrospinal Fluid Leak Suturable DuraGen™ | IART Integra LifeSciences Corporation | — | Completed | 106 | Jul 31, 2024 | Registry ↗ |
| Feb 14, 2025 | The SurgiMend PRS Retrospective Study NCT05182177 · Reconstructive Surgical Procedures SurgiMend PRS | IART Integra LifeSciences Corporation | — | Completed | 84 | Dec 31, 2024 | Registry ↗ |
| Jan 27, 2025 | Bactiseal Catheter Safety Registry Study NCT06276543 · Hydrocephalus antibiotic-impregnated catheter | IART Integra LifeSciences Corporation | — | Recruiting | 200 | Jul 31, 2026 | Registry ↗ |
| Sep 19, 2024 | Cavitronic Ultrasonic Surgical Aspiration (CUSA) Women's Health Study NCT06297187 · Vulvar Intraepithelial Neoplasia, Condylomata Acuminata CUSA (Cavitronic Ultrasonic Surgical Aspirator) | IART Integra LifeSciences Corporation | — | Completed | 56 | Jul 31, 2024 | Registry ↗ |
| Aug 6, 2024 | Tympanostomy Tube Placement in Children in the Office (Inova Study) NCT01496287 · Otitis Media Tube Delivery System (TDS) | IART Integra LifeSciences Corporation | Not applicable | Completed | 70 | Apr 2012 | Registry ↗ |
| Aug 6, 2024 | inVENT-In-Office Study NCT01324271 · Otitis Media Acclarent Tympanostomy Tube Delivery system (TTDS) | IART Integra LifeSciences Corporation | Not applicable | Completed | 85 | May 2012 | Registry ↗ |
| Aug 6, 2024 | Evaluation of the Tympanostomy Tube Delivery System NCT01202578 · Otitis Media With Effusion, Acute Otitis Media tympanostomy tube | IART Integra LifeSciences Corporation | Phase 2/3 | Completed | 53 | Nov 2010 | Registry ↗ |
| Aug 6, 2024 | Optimization and Refinement of Technique in In-Office Sinus Dilation 2 NCT01107379 · Sinusitis Relieva Balloon Sinuplasty System | IART Integra LifeSciences Corporation | — | Completed | 203 | Jan 2012 | Registry ↗ |
| Aug 6, 2024 | Clinical Evaluation of the Ethmoid Sinus Spacer NCT01054703 · Sinusitis, Chronic Rhinosinusitis Ethmoid Sinus Spacer | IART Integra LifeSciences Corporation | Not applicable | Terminated | 14 | Nov 1, 2007 | Registry ↗ |
| Aug 6, 2024 | Singapore Tympanostomy Tube Delivery System Study NCT01046877 · Otitis Media Tympanostomy Tube Delivery System | IART Integra LifeSciences Corporation | Not applicable | Completed | 25 | Aug 2010 | Registry ↗ |
| Aug 6, 2024 | Clinical Study of the Tympanostomy Tube Delivery System NCT00939796 · Otitis Media With Effusion Acclarent Tympanostomy Tube Delivery System | IART Integra LifeSciences Corporation | Not applicable | Completed | 16 | Jun 2009 | Registry ↗ |
| Aug 6, 2024 | Clinical Study of Safety and Efficacy for the Relieva Stratus With Elution of Triamcinolone Acetoni… NCT00791934 · Sinusitis Stratus Microflow Ethmoid Spacer | IART Integra LifeSciences Corporation | Not applicable | Completed | 63 | Nov 2011 | Registry ↗ |
| Aug 6, 2024 | Clinical Evaluation to Confirm Safety and Efficacy of Sinuplasty in the Paranasal Sinuses (CLEAR) NCT00231062 · Chronic Sinusitis Sinuplasty | IART Integra LifeSciences Corporation | Phase 3 | Completed | 115 | Jun 2006 | Registry ↗ |
| Jul 12, 2024 | Global Sinus Surgery Registry NCT02347943 · Chronic Rhinosinusitis, Recurrent Acute Rhinosinusitis | IART Integra LifeSciences Corporation | — | Terminated | 252 | Nov 1, 2015 | Registry ↗ |
| Jul 12, 2024 | Acclarent Tympanostomy Tube Delivery System for the Treatment of Patients Requiring Tympanostomy Tu… NCT02150044 · Otitis Media Acclarent Tympanostomy Tube Delivery System (TTDS). | IART Integra LifeSciences Corporation | Not applicable | Completed | 29 | Oct 2010 | Registry ↗ |
| Jul 12, 2024 | Study of Safety and Efficacy for the Eustachian Tube Balloon Catheter NCT02087150 · Eustachian Tube Dysfunction Acclarent Eustachian Tube Balloon Catheter (ETBC) | IART Integra LifeSciences Corporation | Not applicable | Completed | 323 | Dec 1, 2016 | Registry ↗ |
| Jul 12, 2024 | Comparison of Balloon Sinuplasty In-Office Versus Medical Management for Recurrent Acute Sinusitis… NCT01714687 · Recurrent Acute Rhinosinusitis balloon sinus dilation, medical therapy | IART Integra LifeSciences Corporation | Not applicable | Completed | 59 | Oct 1, 2015 | Registry ↗ |
| Jul 12, 2024 | Medical Therapy Versus Balloon Sinus Dilation for Patients With Chronic Rhinosinusitis NCT01685229 · Sinusitis Balloon sinus dilation, Medical Management | IART Integra LifeSciences Corporation | — | Completed | 198 | Apr 1, 2015 | Registry ↗ |
| Jul 12, 2024 | inVENT-visIOn Study NCT01444391 · Otitis Media Tympanostomy tube placement (Acclarent iontophoresis device) | IART Integra LifeSciences Corporation | Not applicable | Completed | 42 | May 2012 | Registry ↗ |
| Jul 12, 2024 | Anesthetic Effect of Lidocaine/Epinephrine Solution Delivered Via Iontophoresis to External Auditor… NCT00941993 · Acute Otitis Media, Chronic Otitis Media Iontophoresis System (Acclarent) | IART Integra LifeSciences Corporation | Not applicable | Completed | 109 | Jan 2011 | Registry ↗ |
| Jul 12, 2024 | Safety and Efficacy of Balloon Sinuplasty in Pediatric Sinusitis NCT00939471 · Chronic Sinusitis Relieva™ Balloon Sinuplasty™ System | IART Integra LifeSciences Corporation | Not applicable | Completed | 44 | Jul 1, 2009 | Registry ↗ |
| Jul 12, 2024 | Balloon Sinus Dilation In Office or OR NCT00939393 · Chronic Sinusitis FESS instruments with or without balloon treatment, Balloon… | IART Integra LifeSciences Corporation | Not applicable | Completed | 72 | Jun 1, 2009 | Registry ↗ |
| Jul 11, 2024 | REINVENT Registry (Registry of the Nerve Gap Repair From Integra) NCT05339594 · Peripheral Nerve Injuries NeuraGen, NeuraGen 3D | IART Integra LifeSciences Corporation | — | Terminated | 17 | Jun 3, 2024 | Registry ↗ |
| Jul 11, 2024 | Earset Healthy Volunteer Study NCT01611246 · Otitis Media Iontophoresis System With Earset | IART Integra LifeSciences Corporation | — | Completed | 22 | Aug 1, 2012 | Registry ↗ |
| Jul 11, 2024 | Canadian Health Economics, Outcome, and Effectiveness Comparison of Treatment in Patients With Chro… NCT01455948 · Chronic Rhinosinusitis Relieva Balloon Sinuplasty™ System, Functional Endoscopic S… | IART Integra LifeSciences Corporation | Not applicable | Terminated | 25 | Nov 2012 | Registry ↗ |
| Jul 11, 2024 | Healthy Volunteer Study NCT01346332 · Anesthesia of Tympanic Membrane Iontophoresis System with Headset | IART Integra LifeSciences Corporation | — | Completed | 106 | Feb 1, 2012 | Registry ↗ |
| Jul 11, 2024 | Anesthetizing the Tympanic Membrane in Healthy Volunteers NCT01047904 · Evaluate Performance and Reliability of Iontophoresis System Acclarent Iontophoresis System | IART Integra LifeSciences Corporation | Not applicable | Completed | 21 | Nov 2009 | Registry ↗ |
| Jun 18, 2024 | Gentrix® Surgical Matrix for Soft Tissue Reinforcement in Ventral Hernia Repair NCT05610267 · Ventral Hernia Retrospective chart review | IART Integra LifeSciences Corporation | — | Completed | 28 | Dec 28, 2022 | Registry ↗ |
| May 16, 2024 | NeuraGen 3D Pilot Study NCT05343143 · Digital Nerve Injury NeuraGen 3D Nerve Guide Matrix | IART Integra LifeSciences Corporation | Not applicable | Terminated | 1 | Jul 11, 2023 | Registry ↗ |
| Apr 1, 2024 | A Multi-center, Prospective, Randomized Study With PriMatrix and PriMatrix Ag for the Treatment of… NCT01612806 · Venous Stasis Ulcer PriMatrix, PriMatrix Ag | IART Integra LifeSciences Corporation | Not applicable | Terminated | 31 | Feb 2017 | Registry ↗ |
| Aug 7, 2023 | The CUSA Clarity Bone Tip Study NCT04300075 · Cranial Skull Base Bone Removal CUSABT | IART Integra LifeSciences Corporation | — | Withdrawn | 0 | Aug 2024 | Registry ↗ |
| Mar 28, 2023 | Bactiseal Catheter Safety Registry in China NCT04496414 · Hydrocephalus Bactiseal Catheter | IART Integra LifeSciences Corporation | — | Completed | 50 | Nov 30, 2020 | Registry ↗ |
| Apr 29, 2022 | PriMatrix for the Management of Diabetic Foot Ulcers NCT03010319 · Diabetic Foot Ulcer PriMatrix Dermal Repair Scaffold, Secondary Dressings | IART Integra LifeSciences Corporation | Not applicable | Completed | 226 | Aug 2020 | Registry ↗ |
| Feb 8, 2022 | The CUSA Clarity Soft Tissue Removal Study NCT04298268 · Benign, Malignant Tumors or Other Soft Tissue Removal, Neph… CUSA Clarity Ultrasonic Surgical Aspirator System use | IART Integra LifeSciences Corporation | — | Completed | 100 | Nov 24, 2021 | Registry ↗ |
| Feb 8, 2022 | ACell MatriStem Pelvic Floor Matrix Versus Native Tissue Repair, Comparative Study NCT02021279 · Pelvic Organ Prolapse MatriStem Pelvic Floor Matrix, native tissue repair | IART Integra LifeSciences Corporation | Not applicable | Completed | 161 | Apr 28, 2021 | Registry ↗ |
| Jan 26, 2022 | CERTAS Programmable Valve Registry NCT04207229 · Hydrocephalus, NPH (Normal Pressure Hydrocephalus) CODMAN CERTAS Programmable Valves | IART Integra LifeSciences Corporation | — | Completed | 35 | Nov 18, 2021 | Registry ↗ |
| Jan 14, 2022 | Sundt™ Carotid Shunt Retrospective Post Market Clinical Follow-up Study (PMCF) NCT03816202 · Carotid Artery Stenosis Sundt carotid shunt | IART Integra LifeSciences Corporation | — | Completed | 100 | Aug 27, 2019 | Registry ↗ |
| Nov 5, 2021 | A Study on the Safety of Hakim Programmable Shunt System NCT04285489 · Hydrocephalus Hakim Shunt Programmable System | IART Integra LifeSciences Corporation | — | Completed | 130 | Jul 28, 2020 | Registry ↗ |
| Nov 2, 2021 | AmnioExcel® Plus vs SOC in the Management of Diabetic Foot Ulcers NCT05024656 · Diabetic Foot Ulcer AmnioExcel Plus Amniotic Membrane, Standard of Care | IART Integra LifeSciences Corporation | Not applicable | Withdrawn | 0 | Feb 2024 | Registry ↗ |
| Aug 25, 2021 | Diabetic Foot Ulcer Study Comparing Cytal Wound Matrix 1-Layer to Standard of Care NCT03626623 · Diabetes, Diabetic Foot Cytal Wound Matrix 1-Layer, Standard of Care (SOC) | IART Integra LifeSciences Corporation | Not applicable | Terminated | 15 | Feb 18, 2020 | Registry ↗ |
The newest 50 items, most recent first. Each row links to the study's page on ClinicalTrials.gov. Updated Nov 15, 2026, 6:15 PM EST.
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