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COMPANY

ConvaTec

HQ: London, United Kingdom source · convatec.com ↗

FDA-cleared device company Past trials only

Location: London, United Kingdom · source · Oct 14, 2026

Profile checked Oct 10, 2026

Keywords: Wound Heal Ileostomy Colostomy Venous Leg Ulcer Diabetic Foot Diabetic Foot Ulcer Ostomy Leg Ulcers Urostomy Wound Infection Multiple Sclerosis Spinal Cord Injuries Trauma-related Wound Ulcer Diabetic Foot Ulcers Ulcer Foot Ulcer Healing Wound Healing Venous Ulcer Ulcer Venous Colostomy Stoma Ileostomy - Stoma Bladder Outlet Obstruction Cauda Equina Syndrome Enlarged Prostate With Lower Urinary Tract Symptoms Parkinson Disease Lower Urinary Tract Symptoms Detrusor Underactivity Recent Surgical Wound Surgical Wound Leak Dehiscence Wound Neurogenic Bladder Chronic Ulcer of Leg or Foot Pressure Injury Surgical Wound Skin Breakdown End Colostomy Comfort and Performance of Intermittent Catheter Parkinsonian Disorders

46Trials (company is sponsor)

Timeline

  1. Trial start —: A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers. source ↗
  2. Trial start Not phased (device or behavioral study): ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic Wounds source ↗
  3. Trial start Not phased (device or behavioral study): EDX110 Randomized Control Trial for Treatment of DFUs source ↗
  4. Trial start —: AQUACEL® Ag+ Extra™ vs Cutimed® Sorbact® source ↗
  5. Trial start Not phased (device or behavioral study): IDEAL: Efficacy of Porcine Placental Extracellular Matrix Augmented Plus Standard of Care (SOC) Versus SOC Alone for the Management of Diabetic Foot Ulcers source ↗
  6. Trial start —: SCOPE - Single-Point Classification Observational Peristomal Evaluation source ↗
  7. Trial start Not phased (device or behavioral study): EDX110 - Efficacy and Safety in the Management of Hard-to-heal Wounds source ↗
  8. Trial start Not phased (device or behavioral study): INNOVEN: Efficacy of Porcine Placental Extracellular Matrix Plus Standard of Care (SOC) Versus SOC Alone source ↗
  9. Trial start Not phased (device or behavioral study): Study to Demonstrate the Efficacy and Safety of Convatec ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-adhesive Dressings to Protect Against Skin Breakdown source ↗
  10. Trial start —: A Retrospective, Observational Study of the Real-world Safety and Performance of InnovaMatrix® AC at a Single Centre source ↗
  11. Trial start —: Study of Avelle™ Negative Pressure Wound Therapy (NPWT) System source ↗
  12. Trial start —: Observational Study to Investigate the Use of Sterilized Porcine Placental Tissue in the Treatment of Chronic VLU source ↗
  13. Trial start Not phased (device or behavioral study): A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Performance and Safety of ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-Adhe source ↗
  14. Trial start Not phased (device or behavioral study): A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Safety, and Performance of ConvaFoam™ Dressings in the Management of Indicated Chronic W source ↗
  15. Trial start —: GentleCath™ for Men Intermittent Catheter With FeelClean™ Technology source ↗
  16. Trial start Not phased (device or behavioral study): AQUACEL® Ag+ Extra™ and Cutimed™ Sorbact® Dressing in the Management of Venous Leg Ulcers Over a 12-week Period source ↗
  17. Trial start Not phased (device or behavioral study): Sterilised, Porcine Placental Tissue in the Treatment of Chronic Diabetic Foot Ulcers source ↗
  18. Trial start —: Assessment of Novel Technology to Facilitate Drainage in Ostomy Pouches: OUTFLOW Study source ↗
  19. Trial start —: The Avelle® Negative Pressure Wound Therapy System on Chronic Wounds source ↗
  20. Trial start —: GentleCath™ Air Intermittent Catheter Smartwatch Real Life Pilot Study source ↗
  21. Trial start —: Analytical Performance of pH, HNE and MPO Levels in Detecting Wound Infection Proof of Concept Biomarker Study source ↗
  22. Trial start —: GentleCath Air (Urinary Self-catheterization) - Pain in Female Patients With Neurological Vesico-sphincter Disorders source ↗
  23. Trial start Not phased (device or behavioral study): A Multi-centre Clinical Investigation to Assess the Performance of GentleCath™ Glide Intermittent Catheters source ↗
  24. Trial start —: Aquacel With Strengthening Fiber (WSF) Ribbon Dressings source ↗
  25. Trial start —: User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™ source ↗

Showing 25 of 46 dated events.

Upcoming milestones

Estimated primary completion per ClinicalTrials.gov. Dates move.

Clinical trials (lead sponsor) 46

RecordTitlePhaseStatusStartPrimary completion
NCT06616844IDEAL: Efficacy of Porcine Placental Extracellular Matrix Augmented Plus Standard of Care (SOC) Versus SOC Alone for the Management of Diabetic Foot UlcersNot phased (device or behavioral study)RecruitingFeb 12, 20252027-05 (estimated)
NCT07342049ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic WoundsNot phased (device or behavioral study)RecruitingJan 12, 2026Oct 30, 2026 (estimated)
NCT07438951A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers.Not listedNot yet recruiting2026-072027-09 (estimated)
NCT06614491SCOPE - Single-Point Classification Observational Peristomal EvaluationNot listedCompletedDec 6, 2024Dec 31, 2025 (actual)
NCT07308678AQUACEL® Ag+ Extra™ vs Cutimed® Sorbact®Not listedCompletedApr 22, 2025May 28, 2025 (actual)
NCT07308665Aquacel With Strengthening Fiber (WSF) Ribbon DressingsNot listedCompletedJan 1, 2017Apr 8, 2025 (actual)
NCT06640985EDX110 - Efficacy and Safety in the Management of Hard-to-heal WoundsNot phased (device or behavioral study)Active, not recruitingDec 4, 20242026-02 (estimated)
NCT07209358EDX110 Randomized Control Trial for Treatment of DFUsNot phased (device or behavioral study)RecruitingOct 30, 2025Dec 1, 2026 (estimated)
NCT05666570The Avelle® Negative Pressure Wound Therapy System on Chronic WoundsNot listedWithdrawnMay 18, 2022Nov 27, 2022 (actual)
NCT05892341AQUACEL® Ag+ Extra™ and Cutimed™ Sorbact® Dressing in the Management of Venous Leg Ulcers Over a 12-week PeriodNot phased (device or behavioral study)CompletedDec 5, 2022Feb 14, 2024 (actual)
NCT07170566A Retrospective, Observational Study of the Real-world Safety and Performance of InnovaMatrix® AC at a Single CentreNot listedCompletedMay 1, 2024Jun 5, 2025 (actual)
NCT06606210INNOVEN: Efficacy of Porcine Placental Extracellular Matrix Plus Standard of Care (SOC) Versus SOC AloneNot phased (device or behavioral study)RecruitingSep 19, 20242025-12 (estimated)
NCT05687656Sterilised, Porcine Placental Tissue in the Treatment of Chronic Diabetic Foot UlcersNot phased (device or behavioral study)Active, not recruitingOct 6, 2022Dec 31, 2025 (estimated)
NCT06400875Observational Study to Investigate the Use of Sterilized Porcine Placental Tissue in the Treatment of Chronic VLUNot listedActive, not recruitingJul 10, 2023Dec 31, 2025 (estimated)
NCT06394115Assessment of Novel Technology to Facilitate Drainage in Ostomy Pouches: OUTFLOW StudyNot listedCompletedAug 1, 2022Mar 30, 2023 (actual)
NCT05470751GentleCath™ for Men Intermittent Catheter With FeelClean™ TechnologyNot listedCompletedFeb 2, 2023Apr 6, 2024 (actual)
NCT05805046Study of Avelle™ Negative Pressure Wound Therapy (NPWT) SystemNot listedWithdrawnSep 30, 2023Oct 30, 2023 (actual)
NCT05683938GentleCath™ Air Intermittent Catheter Smartwatch Real Life Pilot StudyNot listedCompletedNov 18, 2021Apr 26, 2023 (actual)
NCT05632250A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Safety, and Performance of ConvaFoam™ Dressings in the Management of Indicated Chronic Wound Types.Not phased (device or behavioral study)CompletedApr 10, 2023Mar 13, 2024 (actual)
NCT05632276A Prospective, Multi Centre, Interventional, Non-comparator, Open Label Study to Demonstrate the Efficacy, Performance and Safety of ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-Adhesive Dressings in the Management of Surgical and Traumatic WoundsNot phased (device or behavioral study)CompletedJun 8, 2023Mar 13, 2024 (actual)
NCT05902182Study to Demonstrate the Efficacy and Safety of Convatec ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-adhesive Dressings to Protect Against Skin BreakdownNot phased (device or behavioral study)Unknown status (ClinicalTrials.gov)2024-072024-12 (estimated)
NCT01138709Vitala 12 Hour Wear Test With Convex ProductsNot phased (device or behavioral study)Completed2010-022010-04 (actual)
NCT01207479Study to Assess the Safety and Performance of The VitalaTM Continence Control Device With Natura Moldable Skin BarriersNot phased (device or behavioral study)Completed2010-092010-11 (actual)
NCT01691729Comparison Study of 3 Ostomy ProductsNot phased (device or behavioral study)Completed2012-092012-11 (actual)
NCT03387878A Multi-centre Clinical Investigation to Assess the Performance of GentleCath™ Glide Intermittent CathetersNot phased (device or behavioral study)CompletedJul 1, 2017Jan 10, 2018 (actual)
NCT04979637Analytical Performance of pH, HNE and MPO Levels in Detecting Wound Infection Proof of Concept Biomarker StudyNot listedWithdrawnJul 1, 2021Nov 1, 2021 (actual)
NCT04847609GentleCath Air (Urinary Self-catheterization) - Pain in Female Patients With Neurological Vesico-sphincter DisordersNot listedWithdrawnMay 31, 2021Sep 1, 2021 (actual)
NCT01897285A Single Centre, Randomised, Comparative, Blinded Wear Test of Two Adhesives on the AQUACEL® Foam Adhesive DressingNot phased (device or behavioral study)Completed2013-052013-05 (actual)
NCT00821808A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy VolunteersPhase 1Completed2008-052008-06 (actual)
NCT02499588User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™Not listedUnknown status (ClinicalTrials.gov)2015-062016-08 (estimated)
NCT00821431Compression Device Versus 4-layer Compression SystemPhase 2Completed2006-052008-06 (actual)
NCT01939106One Piece Drainable Pouch in Subjects With an IleostomyPhase 2Completed2013-062013-06 (actual)
NCT01935999One Piece Closed Pouch in Subjects With a ColostomyPhase 2Completed2013-062013-07 (actual)
NCT01427491Compare Aquacel® Ag Versus Mepilex® Border Ag to Manage Bioburden in Leg UlcersPhase 3Completed2011-082012-01 (actual)
NCT01591434Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg UlcersPhase 3Completed2012-052012-09 (actual)
NCT01782196A Phase II Multi Centre Study to Assess the Safety and Performance of Two Prototype One Piece Pouches in Subjects With an IleostomyIITerminated2012-102013-03 (actual)
NCT01526967Observational Evaluation of the Peristomal Skin Condition in OstomatesNot listedUnknown status (ClinicalTrials.gov)2012-012012-12 (estimated)
NCT01590368A Comparative Wear Test of Two Adhesives on the Unilect ™ Biotab Short Term Monitoring ElectrodePhase 3Unknown status (ClinicalTrials.gov)2012-062012-06 (estimated)
NCT01497210EASH Dressing on Chronic Venous Leg UlcersPhase 2Completed2011-112012-04 (actual)
NCT01084577AQUACEL® Ag Dressing and Urgotul® Silver Dressing on Healing of Chronic Venous Leg UlcersPhase 4Completed2010-012011-01 (actual)
NCT01261988Assess the Safety and Adhesive Performance of the VIPER System When Compared to Esteem™Phase 1Completed2010-122010-12 (actual)
NCT00902252Multi-National Phase III Vitala™ 12-Hour Wear TestIIICompleted2009-042010-01 (actual)
NCT01081522A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute WoundsNot listedCompleted2009-102010-02 (actual)
NCT00731367Comparative Evaluation of Two AQUACEL Ag Protocols of Care for the Management of Donor SitesPhase 3Completed2005-102006-07 (actual)
NCT00732719Compression Device Safety Study on EdemaPhase 2Completed2004-102004-11 (actual)
NCT00732823Compression Device Safety StudyPhase 2Completed2005-072005-10 (actual)
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