Our grouping. This page groups the registry's lead sponsor names by company — our grouping, not the registry's. It can be wrong or incomplete: an acquired company whose name never mentions its owner may be missing. Use “Something wrong?” under any name below to correct it.
Tell us about a missing company
ConvaTec Inc. clinical trials
The registry lists 46 studies whose lead sponsor is ConvaTec Inc.. 5 are recruiting or about to start. Per ClinicalTrials.gov, last updated Oct 22, 2026.
Keep track of what changes. Save the ConvaTec Inc. studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesRegistry sponsor names on this page
Each name exactly as ClinicalTrials.gov lists it, and how it relates to ConvaTec Inc..
- ConvaTec Inc.46 studiesSame company
Something wrong?
Focus areas
Conditions ConvaTec Inc. leads ten or more studies in, by study count. A broader condition is left out when almost all its studies are already in a narrower one listed here.
Studies
Recruiting first, then most recently updated. Showing 46 of 46.
- ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic WoundsRecruitingNCT07342049Not applicable
- A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers.Not yet recruitingNCT07438951
- EDX110 Randomized Control Trial for Treatment of DFUsRecruitingNCT07209358Not applicable
- INNOVEN: Efficacy of Porcine Placental Extracellular Matrix Plus Standard of Care (SOC) Versus SOC AloneRecruitingNCT06606210Not applicable
- Study to Demonstrate the Efficacy and Safety of Convatec ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-adhesive Dressings to Protect Against Skin BreakdownNot yet recruitingNCT05902182Not applicable
- IDEAL: Efficacy of Porcine Placental Extracellular Matrix Augmented Plus Standard of Care (SOC) Versus SOC Alone for the Management of Diabetic Foot UlcersActive, not recruitingNCT06616844Not applicable
- SCOPE - Single-Point Classification Observational Peristomal EvaluationCompletedNCT06614491
- AQUACEL® Ag+ Extra™ vs Cutimed® Sorbact®CompletedNCT07308678
- Aquacel With Strengthening Fiber (WSF) Ribbon DressingsCompletedNCT07308665
- EDX110 - Efficacy and Safety in the Management of Hard-to-heal WoundsActive, not recruitingNCT06640985Not applicable
- The Avelle® Negative Pressure Wound Therapy System on Chronic WoundsWithdrawnNCT05666570
- AQUACEL® Ag+ Extra™ and Cutimed™ Sorbact® Dressing in the Management of Venous Leg Ulcers Over a 12-week PeriodCompletedNCT05892341Not applicable
- A Retrospective, Observational Study of the Real-world Safety and Performance of InnovaMatrix® AC at a Single CentreCompletedNCT07170566
- Sterilised, Porcine Placental Tissue in the Treatment of Chronic Diabetic Foot UlcersActive, not recruitingNCT05687656Not applicable
- Observational Study to Investigate the Use of Sterilized Porcine Placental Tissue in the Treatment of Chronic VLUActive, not recruitingNCT06400875
- Assessment of Novel Technology to Facilitate Drainage in Ostomy Pouches: OUTFLOW StudyCompletedNCT06394115
- 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-Adhesive Dressings in the Management of Surgical and Traumatic WoundsCompletedNCT05632276Not applicable
- Study of Avelle™ Negative Pressure Wound Therapy (NPWT) SystemWithdrawnNCT05805046
- GentleCath™ Air Intermittent Catheter Smartwatch Real Life Pilot StudyCompletedNCT05683938
- 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 Wound Types.CompletedNCT05632250Not applicable
- GentleCath™ for Men Intermittent Catheter With FeelClean™ TechnologyCompletedNCT05470751
- Comparison Study of 3 Ostomy ProductsCompletedNCT01691729Not applicable
- Vitala 12 Hour Wear Test With Convex ProductsCompletedNCT01138709Not applicable
- Study to Assess the Safety and Performance of The VitalaTM Continence Control Device With Natura Moldable Skin BarriersCompletedNCT01207479Not applicable
- A Multi-centre Clinical Investigation to Assess the Performance of GentleCath™ Glide Intermittent CathetersCompletedNCT03387878Not applicable
- Analytical Performance of pH, HNE and MPO Levels in Detecting Wound Infection Proof of Concept Biomarker StudyWithdrawnNCT04979637
- GentleCath Air (Urinary Self-catheterization) - Pain in Female Patients With Neurological Vesico-sphincter DisordersWithdrawnNCT04847609
- A Single Centre, Randomised, Comparative, Blinded Wear Test of Two Adhesives on the AQUACEL® Foam Adhesive DressingCompletedNCT01897285Not applicable
- A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy VolunteersCompletedNCT00821808Phase 1
- User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™Status unknownNCT02499588
- Compression Device Versus 4-layer Compression SystemCompletedNCT00821431Phase 2
- One Piece Drainable Pouch in Subjects With an IleostomyCompletedNCT01939106Phase 2
- One Piece Closed Pouch in Subjects With a ColostomyCompletedNCT01935999Phase 2
- Compare Aquacel® Ag Versus Mepilex® Border Ag to Manage Bioburden in Leg UlcersCompletedNCT01427491Phase 3
- Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg UlcersCompletedNCT01591434Phase 3
- A Phase II Multi Centre Study to Assess the Safety and Performance of Two Prototype One Piece Pouches in Subjects With an IleostomyTerminatedNCT01782196Not applicable
- Observational Evaluation of the Peristomal Skin Condition in OstomatesStatus unknownNCT01526967
- A Comparative Wear Test of Two Adhesives on the Unilect ™ Biotab Short Term Monitoring ElectrodeStatus unknownNCT01590368Phase 3
- EASH Dressing on Chronic Venous Leg UlcersCompletedNCT01497210Phase 2
- AQUACEL® Ag Dressing and Urgotul® Silver Dressing on Healing of Chronic Venous Leg UlcersCompletedNCT01084577Phase 4
- Assess the Safety and Adhesive Performance of the VIPER System When Compared to Esteem™CompletedNCT01261988Phase 1
- Multi-National Phase III Vitala™ 12-Hour Wear TestCompletedNCT00902252Phase 3
- A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute WoundsCompletedNCT01081522
- Comparative Evaluation of Two AQUACEL Ag Protocols of Care for the Management of Donor SitesCompletedNCT00731367Phase 3
- Compression Device Safety Study on EdemaCompletedNCT00732719Phase 2
- Compression Device Safety StudyCompletedNCT00732823Phase 2