CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 40 enrolled
Drug / intervention
Platelet Rich Plasma +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07456215
NCT07456215Phase 1Completed

The Effect of Platelet Rich Plasma (PRP) Application on Rotator Cuff Tear.

Aristotle University Of Thessaloniki·interventional·Posted Mar 6, 2026·Updated Mar 6, 2026

In Brief

A Phase 1 clinical trial evaluating Platelet Rich Plasma and Normal saline for Tendon Injuries and 2 related conditions. Completed, enrolled 40 participants across 1 site.

Detailed Summary

The aim of this randomized control trial is to evaluate the impact and effectiveness of PRP on tenocyte metabolism and tendon tissue properties in rotator cuff tear.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesGreece
Collaborators--

Timeline

Phase 1CompletedFinished
2023202420252026
First PostedMar 6, 2026
Enrollment StartDec 23, 2022
Primary CompletionJan 13, 2026
Study CompletionJan 14, 2026
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 4 months ago

Interventions

Platelet Rich Plasmabiological

The injection of PRP in the subacromial space.

Normal salineother

The injection of normal saline in the subacromial space.