UnknownPhase 4

Rotator Cuff Tendinopathy Conservative Treatment With Collagen, PRP or Both

Poland90 participantsStarted 2020-07-01

Plain-language summary

The aim of the trial is comparison of the effectiveness of three methods of conservative treatment in partial thickness rotator cuff injury (PTRCI): collagen with PRP injections, PRP injections alone and collagen injections alone.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * clinical signs and symptoms of rotator cuff pathology * an adult person consenting to injections * partial thickness rotator cuff injury confirmed by ultrasound examination without coexisting severe pathologies (systemic inflammatory disease, malignancy, severe stage OA) * no traumatic event * no injections or any other local treatment in previous 1 month Exclusion Criteria: * full thickness rotator cuff injury * acute, traumatic injuries requiring surgical treatment * coexisting injuries of the shoulder joint requiring other intervention * severe pathologies of the shoulder of another origin (systemic inflammatory disease, malignancy, severe stage OA) * no consent

What they're measuring

Change in EQ-5D-5L index from baseline to 24 week

Timeframe: Change from baseline to 24 weeks

QuickDASH (Disabilities of Arm, Shoulder and Hand) questionnaire summary score change from baseline to 24 weeks

Timeframe: Change from baseline to 24 weeks

Trial details

NCT IDNCT04492748

SponsorSutherland Medical Center

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2021-09-30

View on ClinicalTrials.gov More Rotator Cuff Tendinosis trials