Trials / Completed
CompletedNCT05458349
Acellular Dermis in Rotator Cuff Repair
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 63 (actual)
- Sponsor
- The Royal Orthopaedic Hospital NHS Trust · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To determine if an acellular dermal graft (ADG) will incorporate into the rotator cuff and subsequently improve outcomes without an increase in risk to the patient
Detailed description
Rotator cuff healing poses a significant clinical problem with re-tear rates between 20-50%. The final functional outcome following surgery correlates with healing, with those that completely heal performing best. Failure of repair is mainly due to tendon failure both mechanically and biologically. If the healing and the structural properties of the tendon can be improved then significant functional gains may be achieved. This study will therefore utilise acellular dermal grafts to determine whether they could be used for to improve patient outcomes following surgery
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | acellular dermis |
Timeline
- Start date
- 2013-04-04
- Primary completion
- 2021-02-11
- Completion
- 2021-02-11
- First posted
- 2022-07-14
- Last updated
- 2022-07-14
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT05458349. Inclusion in this directory is not an endorsement.