COMPANY
ConvaTec
FDA-cleared device company Past trials only
Timeline
- Trial start —: A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers. source ↗
- Trial start Not phased (device or behavioral study): ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic Wounds source ↗
- Trial start Not phased (device or behavioral study): EDX110 Randomized Control Trial for Treatment of DFUs source ↗
- Trial start —: AQUACEL® Ag+ Extra™ vs Cutimed® Sorbact® source ↗
- 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 ↗
- Trial start —: SCOPE - Single-Point Classification Observational Peristomal Evaluation source ↗
- Trial start Not phased (device or behavioral study): EDX110 - Efficacy and Safety in the Management of Hard-to-heal Wounds source ↗
- Trial start Not phased (device or behavioral study): INNOVEN: Efficacy of Porcine Placental Extracellular Matrix Plus Standard of Care (SOC) Versus SOC Alone source ↗
- 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 ↗
- Trial start —: A Retrospective, Observational Study of the Real-world Safety and Performance of InnovaMatrix® AC at a Single Centre source ↗
- Trial start —: Study of Avelle™ Negative Pressure Wound Therapy (NPWT) System source ↗
- Trial start —: Observational Study to Investigate the Use of Sterilized Porcine Placental Tissue in the Treatment of Chronic VLU source ↗
- 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 ↗
- 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 ↗
- Trial start —: GentleCath™ for Men Intermittent Catheter With FeelClean™ Technology source ↗
- 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 ↗
- Trial start Not phased (device or behavioral study): Sterilised, Porcine Placental Tissue in the Treatment of Chronic Diabetic Foot Ulcers source ↗
- Trial start —: Assessment of Novel Technology to Facilitate Drainage in Ostomy Pouches: OUTFLOW Study source ↗
- Trial start —: The Avelle® Negative Pressure Wound Therapy System on Chronic Wounds source ↗
- Trial start —: GentleCath™ Air Intermittent Catheter Smartwatch Real Life Pilot Study source ↗
- Trial start —: Analytical Performance of pH, HNE and MPO Levels in Detecting Wound Infection Proof of Concept Biomarker Study source ↗
- Trial start —: GentleCath Air (Urinary Self-catheterization) - Pain in Female Patients With Neurological Vesico-sphincter Disorders source ↗
- Trial start Not phased (device or behavioral study): A Multi-centre Clinical Investigation to Assess the Performance of GentleCath™ Glide Intermittent Catheters source ↗
- Trial start —: Aquacel With Strengthening Fiber (WSF) Ribbon Dressings source ↗
- Trial start —: User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™ source ↗
Upcoming milestones
- Oct 30, 2026 (ESTIMATED) · Not phased · ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic Wounds · NCT07342049
- Dec 1, 2026 (ESTIMATED) · Not phased · EDX110 Randomized Control Trial for Treatment of DFUs · NCT07209358
- 2027-05 (ESTIMATED) · Not phased · IDEAL: Efficacy of Porcine Placental Extracellular Matrix Augmented Plus Standard of Care (SOC) Versus SOC Alone for the Management of Diabetic Foot Ulcers · NCT06616844
- 2027-09 (ESTIMATED) · · A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers. · NCT07438951
Clinical trials (lead sponsor) 46
| Record | Title | Phase | Status | Start | Primary completion |
|---|---|---|---|---|---|
| NCT06616844 | IDEAL: Efficacy of Porcine Placental Extracellular Matrix Augmented Plus Standard of Care (SOC) Versus SOC Alone for the Management of Diabetic Foot Ulcers | Not phased (device or behavioral study) | Recruiting | Feb 12, 2025 | 2027-05 (estimated) |
| NCT07342049 | ConvaVAC™ Ag+ Negative Pressure Wound Therapy System in Chronic Wounds | Not phased (device or behavioral study) | Recruiting | Jan 12, 2026 | Oct 30, 2026 (estimated) |
| NCT07438951 | A Study on the Efficacy and Safety of a Nitric Oxide Generating Dressing in the Treatment of Diabetes Related Foot Ulcers. | Not listed | Not yet recruiting | 2026-07 | 2027-09 (estimated) |
| NCT06614491 | SCOPE - Single-Point Classification Observational Peristomal Evaluation | Not listed | Completed | Dec 6, 2024 | Dec 31, 2025 (actual) |
| NCT07308678 | AQUACEL® Ag+ Extra™ vs Cutimed® Sorbact® | Not listed | Completed | Apr 22, 2025 | May 28, 2025 (actual) |
| NCT07308665 | Aquacel With Strengthening Fiber (WSF) Ribbon Dressings | Not listed | Completed | Jan 1, 2017 | Apr 8, 2025 (actual) |
| NCT06640985 | EDX110 - Efficacy and Safety in the Management of Hard-to-heal Wounds | Not phased (device or behavioral study) | Active, not recruiting | Dec 4, 2024 | 2026-02 (estimated) |
| NCT07209358 | EDX110 Randomized Control Trial for Treatment of DFUs | Not phased (device or behavioral study) | Recruiting | Oct 30, 2025 | Dec 1, 2026 (estimated) |
| NCT05666570 | The Avelle® Negative Pressure Wound Therapy System on Chronic Wounds | Not listed | Withdrawn | May 18, 2022 | Nov 27, 2022 (actual) |
| NCT05892341 | AQUACEL® Ag+ Extra™ and Cutimed™ Sorbact® Dressing in the Management of Venous Leg Ulcers Over a 12-week Period | Not phased (device or behavioral study) | Completed | Dec 5, 2022 | Feb 14, 2024 (actual) |
| NCT07170566 | A Retrospective, Observational Study of the Real-world Safety and Performance of InnovaMatrix® AC at a Single Centre | Not listed | Completed | May 1, 2024 | Jun 5, 2025 (actual) |
| NCT06606210 | INNOVEN: Efficacy of Porcine Placental Extracellular Matrix Plus Standard of Care (SOC) Versus SOC Alone | Not phased (device or behavioral study) | Recruiting | Sep 19, 2024 | 2025-12 (estimated) |
| NCT05687656 | Sterilised, Porcine Placental Tissue in the Treatment of Chronic Diabetic Foot Ulcers | Not phased (device or behavioral study) | Active, not recruiting | Oct 6, 2022 | Dec 31, 2025 (estimated) |
| NCT06400875 | Observational Study to Investigate the Use of Sterilized Porcine Placental Tissue in the Treatment of Chronic VLU | Not listed | Active, not recruiting | Jul 10, 2023 | Dec 31, 2025 (estimated) |
| NCT06394115 | Assessment of Novel Technology to Facilitate Drainage in Ostomy Pouches: OUTFLOW Study | Not listed | Completed | Aug 1, 2022 | Mar 30, 2023 (actual) |
| NCT05470751 | GentleCath™ for Men Intermittent Catheter With FeelClean™ Technology | Not listed | Completed | Feb 2, 2023 | Apr 6, 2024 (actual) |
| NCT05805046 | Study of Avelle™ Negative Pressure Wound Therapy (NPWT) System | Not listed | Withdrawn | Sep 30, 2023 | Oct 30, 2023 (actual) |
| NCT05683938 | GentleCath™ Air Intermittent Catheter Smartwatch Real Life Pilot Study | Not listed | Completed | Nov 18, 2021 | Apr 26, 2023 (actual) |
| NCT05632250 | 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. | Not phased (device or behavioral study) | Completed | Apr 10, 2023 | Mar 13, 2024 (actual) |
| NCT05632276 | 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 Wounds | Not phased (device or behavioral study) | Completed | Jun 8, 2023 | Mar 13, 2024 (actual) |
| NCT05902182 | Study to Demonstrate the Efficacy and Safety of Convatec ConvaFoam™ Silicone, ConvaFoam™ Border and ConvaFoam™ Non-adhesive Dressings to Protect Against Skin Breakdown | Not phased (device or behavioral study) | Unknown status (ClinicalTrials.gov) | 2024-07 | 2024-12 (estimated) |
| NCT01138709 | Vitala 12 Hour Wear Test With Convex Products | Not phased (device or behavioral study) | Completed | 2010-02 | 2010-04 (actual) |
| NCT01207479 | Study to Assess the Safety and Performance of The VitalaTM Continence Control Device With Natura Moldable Skin Barriers | Not phased (device or behavioral study) | Completed | 2010-09 | 2010-11 (actual) |
| NCT01691729 | Comparison Study of 3 Ostomy Products | Not phased (device or behavioral study) | Completed | 2012-09 | 2012-11 (actual) |
| NCT03387878 | A Multi-centre Clinical Investigation to Assess the Performance of GentleCath™ Glide Intermittent Catheters | Not phased (device or behavioral study) | Completed | Jul 1, 2017 | Jan 10, 2018 (actual) |
| NCT04979637 | Analytical Performance of pH, HNE and MPO Levels in Detecting Wound Infection Proof of Concept Biomarker Study | Not listed | Withdrawn | Jul 1, 2021 | Nov 1, 2021 (actual) |
| NCT04847609 | GentleCath Air (Urinary Self-catheterization) - Pain in Female Patients With Neurological Vesico-sphincter Disorders | Not listed | Withdrawn | May 31, 2021 | Sep 1, 2021 (actual) |
| NCT01897285 | A Single Centre, Randomised, Comparative, Blinded Wear Test of Two Adhesives on the AQUACEL® Foam Adhesive Dressing | Not phased (device or behavioral study) | Completed | 2013-05 | 2013-05 (actual) |
| NCT00821808 | A Pressure Relted Study Comparing a Compression Device and Profore® on Healthy Volunteers | Phase 1 | Completed | 2008-05 | 2008-06 (actual) |
| NCT02499588 | User Evaluation of the Peristomal Skin Condition in Ostomates Using ConvaTec Moldable Technology™ | Not listed | Unknown status (ClinicalTrials.gov) | 2015-06 | 2016-08 (estimated) |
| NCT00821431 | Compression Device Versus 4-layer Compression System | Phase 2 | Completed | 2006-05 | 2008-06 (actual) |
| NCT01939106 | One Piece Drainable Pouch in Subjects With an Ileostomy | Phase 2 | Completed | 2013-06 | 2013-06 (actual) |
| NCT01935999 | One Piece Closed Pouch in Subjects With a Colostomy | Phase 2 | Completed | 2013-06 | 2013-07 (actual) |
| NCT01427491 | Compare Aquacel® Ag Versus Mepilex® Border Ag to Manage Bioburden in Leg Ulcers | Phase 3 | Completed | 2011-08 | 2012-01 (actual) |
| NCT01591434 | Study to Evaluate the Performance of AQUACEL® Extra™ in Venous Leg Ulcers | Phase 3 | Completed | 2012-05 | 2012-09 (actual) |
| NCT01782196 | A Phase II Multi Centre Study to Assess the Safety and Performance of Two Prototype One Piece Pouches in Subjects With an Ileostomy | II | Terminated | 2012-10 | 2013-03 (actual) |
| NCT01526967 | Observational Evaluation of the Peristomal Skin Condition in Ostomates | Not listed | Unknown status (ClinicalTrials.gov) | 2012-01 | 2012-12 (estimated) |
| NCT01590368 | A Comparative Wear Test of Two Adhesives on the Unilect ™ Biotab Short Term Monitoring Electrode | Phase 3 | Unknown status (ClinicalTrials.gov) | 2012-06 | 2012-06 (estimated) |
| NCT01497210 | EASH Dressing on Chronic Venous Leg Ulcers | Phase 2 | Completed | 2011-11 | 2012-04 (actual) |
| NCT01084577 | AQUACEL® Ag Dressing and Urgotul® Silver Dressing on Healing of Chronic Venous Leg Ulcers | Phase 4 | Completed | 2010-01 | 2011-01 (actual) |
| NCT01261988 | Assess the Safety and Adhesive Performance of the VIPER System When Compared to Esteem™ | Phase 1 | Completed | 2010-12 | 2010-12 (actual) |
| NCT00902252 | Multi-National Phase III Vitala™ 12-Hour Wear Test | III | Completed | 2009-04 | 2010-01 (actual) |
| NCT01081522 | A Preliminary, Non-comparative Study to Evaluate a Bioresorbable Wound Scaffold in Acute Wounds | Not listed | Completed | 2009-10 | 2010-02 (actual) |
| NCT00731367 | Comparative Evaluation of Two AQUACEL Ag Protocols of Care for the Management of Donor Sites | Phase 3 | Completed | 2005-10 | 2006-07 (actual) |
| NCT00732719 | Compression Device Safety Study on Edema | Phase 2 | Completed | 2004-10 | 2004-11 (actual) |
| NCT00732823 | Compression Device Safety Study | Phase 2 | Completed | 2005-07 | 2005-10 (actual) |