examining of the effect of PRP on improving shoulder function

comparison of the effect of PRP on improving shoulder function in patients with tendinopathy with and without rotator cuff tears

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20230610058440N1

Enrollment

Registered

2023-10-11

Start date

2023-06-20

Completion date

Unknown

Last updated

2023-10-16

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

Conditions

Tendonopathy. Injury, poisoning and certain other consequences of external causes

Interventions

Intervention 1: Intervention group: The recipient of two PRP injections, which includes 4cc of concentrated platelets from 25cc of the patient s centrifuged blood. Intervention 2: Control group: Recip

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients between the ages of 18 and 65 who have shoulder pain during activity and a pain score greater than 5.10

Exclusion criteria

Exclusion criteria: The presence of another cause other than tendon disorders in the shoulder axis

Design outcomes

Primary

Measure	Time frame
Shoulder function score in the Munich questionnaire. Timepoint: At the beginning of the study and 3 and 6 months after PRP injection. Method of measurement: Munich questionnaire.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza Bozorgmanesh

Arak University of Medical Sciences

negin.ahmdvnd98@gmail.com+98 912 528 0241

Outcome results

None listed

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