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Comparison of the effect of platelet-rich plasma (PRP) with physiotherapy on pain and muscle damage and Returning to Sport in athletes with groin adductor muscle injury.

Comparison of the effect of platelet-rich plasma (PRP) with physiotherapy on pain and muscle damage and Returning to Sport in athletes with groin adductor muscle injury.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221218056850N1
Enrollment
20
Registered
2023-04-18
Start date
2023-04-09
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

groin pain. Acute pain due to trauma

Interventions

Intervention 1: Intervention group: They only receive PRP injection and undergo rehabilitation after the injectionThey will only receive one PRP injection with a volume of 3 cc with a 5 cc needle in t

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patient consent to enter the study Second and third degree acute injury of the adductor muscle (based on ultrasound evidence) No injury in other muscles around the pelvis (examination, history, ultrasound)

Exclusion criteria

Exclusion criteria: Failure to perform corrective exercises Absence of more than three physiotherapy sessions Desire not to continue studying

Design outcomes

Primary

MeasureTime frame
Average time to return to activity. Timepoint: One week after the injection and then every week up to six weeks in person, after six weeks up to two weeks by phone, after three months, they undergo a final examination again in person through a physical examination and the pain level of the patients using a VAS from zero to zero. The score is determined. Method of measurement: Visual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRumisa Majdi

Mazandaran University of Medical Sciences

romisa.majdi2019@gmail.com+98 11 3336 1700

Outcome results

None listed

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