Clinical Trials Directory

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

TypeNameDescription
DEVICEacellular 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.

Acellular Dermis in Rotator Cuff Repair (NCT05458349) · Clinical Trials Directory