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Effect of PRP as Therapy for Shoulder Osteoarthritis

A

Ain Shams University

Status

Completed

Conditions

Shoulder Osteoarthritis

Treatments

Procedure: Injection in the intraarticular space of glenohumeral joint

Study type

Interventional

Funder types

Other

Identifiers

NCT05043493
ASU 000017585

Details and patient eligibility

About

Patients with shoulder osteoarthritis are suffering from pain and disabilities which lead to difficulties in life. The presence of platelet-rich plasma as regenerative therapy which helps in healing of damaged tissues like ligaments and joint might be of great benefit in managing such conditions.

Full description

Primary and secondary osteoarthritis of the shoulder occurs due to destruction of the articular surface of the humeral head and glenoid , Patient mainly presented with pain and decreases in the range of motion .

Treatment of shoulder osteoarthritis is often controversial and is typically based on the patient's age, the severity of symptoms, and level of activity, radiographic findings, and medical comorbidities.

The new era of management include regenerative therapy ,Platelet-rich plasma (PRP) is one of the regenerative therapy that prove its effect as injections of a concentration of a patient's own platelets to accelerate the healing of injured tendons, ligaments, muscles and joints.

Enrollment

91 patients

Sex

All

Ages

21+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patient's age: From 21 years.
  • Acute symptoms on a background of at least a 3-month history of chronic pain or swelling of the shoulder joint with radiological confirmed (X-ray or MRI)
  • Mild or moderate osteoarthritis of the shoulder joint according to The Samilson-Prieto classification.
  • Numerical Rating Scale for pain scores greater than five on a 10 scale

Exclusion criteria

  • Under 21 years of age
  • Severe osteoarthritis according to The Samilson-Prieto classification. (Figure 1)
  • Neuropsychiatric disorders.
  • Immunocompromised patients.
  • Active infection or malignancy at the joint.
  • Pregnancy and breastfeeding.
  • Patients may have thrombocytopenia, bleeding disorders, or on anticoagulant therapy.
  • Shoulder surgery within 3 months or inflammatory arthritis; previous infection of the shoulder joint.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

91 participants in 2 patient groups, including a placebo group

Injection (study) group
Active Comparator group
Description:
This group will receive platelet rich plasma (PRP) injection
Treatment:
Procedure: Injection in the intraarticular space of glenohumeral joint
Control group
Placebo Comparator group
Description:
This group will receive normal saline (NS) injection
Treatment:
Procedure: Injection in the intraarticular space of glenohumeral joint

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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