To evaluate the functional outcomes inshoulder impingement syndrometreated with arthroscopic subacromialdecompression and platelet richplasma (PRP) augmentatio
- Conditions
- Health Condition 1: M249- Joint derangement, unspecified
- Registration Number
- CTRI/2024/04/066159
- Lead Sponsor
- Pt BD Sharma PGIMS Rohtak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
The inclusion criteria will be skeletally mature patients with shoulder pain lasting for
atleast 3 months with clinical diagnosis of shoulder impingement syndrome confirmed
with MRI scan.
1. Radicular pain.
2. Presence of pathologies such as frozen shoulder, calcific tendinitis, biceps
subluxation, and a superior labrum anterior posterior lesion.
3. Previous shoulder surgery within last 6 months.
4. Connective tissue disorders such as rheumatoid arthritis, polymyalgia
rheumatica, or fibromyalgia.
5. Full thickness rotator cuff tear on MRI.
6. Ligamentous laxity (positive sulcus test) or shoulder dislocation (positive
apprehension test).
7. Prior corticosteroid injection within 3 months of the study.
8. Haemotological and bleeding diathesis.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Outcome <br/ ><br>will be assessed during follow up period as per VAS Score, Constant Score, UCLA Score.Timepoint: Outcome <br/ ><br>will be assessed during follow up period as per VAS Score, Constant Score, UCLA Score at 3 week, 3 months and 6 months
- Secondary Outcome Measures
Name Time Method Any kind of skin reaction, pain and <br/ ><br>complication will be noted during follow up period.Timepoint: Any kind of skin reaction, pain and <br/ ><br>complication will be noted during follow up period of 3 week, 3 months and 6 months