To Study the Effect of a Blood Product named Platelet Rich Plasma in Shoulder Tendon Injuries .

A Randomized Controlled Study Evaluating Effect of Platelet-Rich Plasma in Rotator Cuff Injuries. - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/062451

Enrollment

Registered

2024-02-08

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Arthroscopic Rotator cuff repair: Patients with Diagnosed Rotator cuff tear will be treated with Arthroscopic Rotator Cuff repair and the outcome will be assessed by various subjectiv

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-60 years, Patients of Partial or Complete Rotator Cuff Tear , Primary , Degenerative or Traumatic Rotator Cuff Injuries

Exclusion criteria

Exclusion criteria: History of shoulder fracture involving humeral head on affected side Previous Operative Intervention of the Ipsilateral Shoulder Rotator Cuff Tear associated with other pathologies Previous infection in the same shoulder Uncontrolled Diabetes Patients with Bleeding tendencies and

Design outcomes

Primary

Measure	Time frame
At the end of study , there might be early relief after PRP infiltration in Arthroscopic Rotator Cuff Repair compared to those treated without PRP infiltration .Timepoint: Pre operatively , post operative management day 0 , 3 months post operative management .	—

Secondary

Measure	Time frame
MRI assessment of Rotator cuffTimepoint: 9 months post operative management	—

Countries

India

Contacts

Public ContactDr Sandeep Shrivastava

Datta Meghe Institute of Higher Education and Research

drsandeepshrivastava@gmail.com9765404068

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026