Skip to content

Study of the effects of local platelet-rich plasma (PRP) injection versus autologous blood injection in patients with lateral epicondylitis

Study of the effects of local platelet-rich plasma (PRP) injection versus autologous blood injection in patients with lateral epicondylitis in PM & R clinic of Modarres hospital from 2011 to 2013

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013052313442N1
Enrollment
45
Registered
2013-06-06
Start date
2016-08-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Lateral epicondylitis. Lateral epicondylitis

Interventions

Intervention 1: An Injection of 2cc PRP or autologous blood. Intervention 2: Rest,Tennis elbow strap,Acetaminophen,Wrist extensors stretching and strengthening exercises.
Treatment - Drugs
Treatment - Other
An Injection of 2cc PRP or autologous blood
Rest,Tennis elbow strap,Acetaminophen,Wrist extensors stretching and strengthening exercises

Sponsors

Ethic committe of faculty of medicine,Shahid beheshti University of Medical siences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: history of chronic (at least 3months) pain or swelling of the lateral epicondyle and pain more than 5 of 10 according to visual analogue scale. Exclusion criteria: systemic disorders such as diabetes, rheumatoid arthritis, hematological diseases (coagulopathy), severe cardiovascular diseases, infections, immunosuppression, patients in therapy with anticoagulants or antiaggregants, the use of NSAIDs in the 2 days before blood donation and patients with Hb values of 10 and platelet values of 100,000/mmc; Pregnancy; vasovagal shock; injection of corticosteroid in since 2 weeks ago;any injection in site of tenderness since 1 month ago;malignancy;history of CTS,cervical radiculopathy or radial neuropathy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 0,1,2 month. Method of measurement: VAS Questionnaire.

Secondary

MeasureTime frame
Elbow function. Timepoint: 0,1,2 month. Method of measurement: Modified Mayo clinic performance index for the elbow Questionnaire.;Pressure pain threshold. Timepoint: 0,1,2 month. Method of measurement: Algometer sundoo.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRosa Rahimi

Shahid Modarres hospital

rosarahimi@gmal.com+98 21220740909

Outcome results

None listed

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