Use of a Treated, Devitalized and Sterile Umbilical Cord Amniotic Membrane in the Treatment of STT Osteoarthritis
NCT06038331 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2025-09-30
Summary
The aim of this open, prospective, multicenter trial is to evaluate the use of a sterile, devitalized, processed umbilical cord amniotic membrane implant placed in joint interposition in the treatment of STT osteoarthritis.
Conditions
- Osteoarthritis Hand
Interventions
- BIOLOGICAL
-
SclerFIX-IP
Decellularized, viro-inactivated, freeze-dried and sterile allogeneic graft of amniotic membrane of umbilical cord used as an interposition implant in the STT joint
Sponsors & Collaborators
-
TBF Genie Tissulaire
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-05-28
- Primary Completion
- 2026-12-31
- Completion
- 2026-12-31
Countries
- France
Study Locations
More Related Trials
-
SoundBite™ Crossing System Pivotal Peripheral CTO Crossing Study
NCT03266835 ·Status: COMPLETED ·Phase: NA
-
Treatment of Dupuytren's Disease With Minimal Invasive Surgery and VIVOSORB® Resorbable Implant Device
NCT03741764 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
RelayPro Thoracic Stent-Graft in Subjects With Thoracic Aortic Aneurysms and Penetrating Atherosclerotic Ulcers
NCT02818972 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Endurant Stent Graft System vs Excluder Endoprothesis: ADVANCE Trial
NCT05378347 ·Status: RECRUITING ·Phase: NA
-
Safety and Feasibility of the Injectable BL-1040 Implant
NCT00557531 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
Study of the Thoraflex™ Hybrid Device for the Treatment of Aneurysm/dissection of the Descending Thoracic Aorta
NCT03735472 ·Status: COMPLETED
-
South American Thoracic Stent-Graft Study
NCT01082172 ·Status: COMPLETED ·Phase: NA
-
BIOTRONIK 4French for AMBulatory Peripheral Intervention
NCT03044002 ·Status: COMPLETED
-
Coarctation Of the Aorta Stent Trial
NCT00552812 ·Status: COMPLETED ·Phase: NA
-
S.M.A.R.T.® Nitinol Self-Expandable Stent in the Treatment of Obstructive Superficial Femoral Artery Disease
NCT00739102 ·Status: COMPLETED ·Phase: NA
-
SEAL™IT: Saccular Endovascular Aneurysm Lattice System Interventional Pivotal Trial
NCT05831202 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Large Diameter Advanta™ V12 Covered Stent Trial for Coarctation of the Aorta
NCT00978952 ·Status: COMPLETED ·Phase: NA
-
Study of the RelayPro Thoracic Stent-Graft in Subjects With an Acute, Complicated Type B Aortic Dissection
NCT03033043 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Medical & Economical Evaluation of Fenestrated & Branched Stent-grafts to Treat Complex Aortic Aneurysms
NCT01168037 ·Status: COMPLETED
-
RESOLUTE ONYX Post-Approval Study
NCT03063749 ·Status: COMPLETED
-
The Merit WRAPSODY™ Endovascular Stent Graft
NCT03644017 ·Status: COMPLETED ·Phase: NA
-
Safety and Effectiveness of Surgeon-Modified Stent Grafts forTreatment of Complex Aortic Aneurysms
NCT05531084 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Physician-Sponsored IDE for the Talent Endoluminal Stent Graft System for the Treatment of Thoracic Lesions
NCT00597870 ·Status: COMPLETED ·Phase: NA
-
Shockwave Coronary Rx Lithoplasty® Study (Disrupt CAD I)
NCT02650128 ·Status: COMPLETED ·Phase: NA
-
Study of the Relay Pro® Thoracic Stent-Graft in Subjects With Traumatic Injury of the Descending Thoracic Aorta
NCT03090230 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
The Merit WRAPSODY Central Feasibility Study
NCT04541576 ·Status: WITHDRAWN ·Phase: NA
-
Symbiot III: A Prospective Randomized Trial Evaluating the Symbiot Covered Stent System in Saphenous Vein Grafts
NCT00283413 ·Status: COMPLETED ·Phase: NA
-
Endovascular Repair of Descending Thoracic Aortic Aneurysms
NCT00802984 ·Status: COMPLETED ·Phase: PHASE4
-
Thoracoabdominal Artery Stent Graft System Exploratory Study
NCT06710938 ·Status: RECRUITING ·Phase: NA
-
The Study to Compare the Cordis SMART™ Stent System With the Bard® Luminexx™ Stent
NCT00235131 ·Status: COMPLETED ·Phase: PHASE4