Health Condition 1: M668- Spontaneous rupture of other tendons
Conditions
Interventions
Intervention1: PRP in patients with shoulder rotator cuff tear: under ultrasound guidance platelet concentrate 5-8 ml will be injected in the area of partial tear of muscles of rotator cuff tear/tendi
Sponsors
Department of Anaesthesia and Intensive Care
Eligibility
Inclusion criteria
Inclusion criteria: Partial rotator cuff tear Visual analogue scale score of more than 3 for more than 3 months Patients who can understand and read Hindi and English
Exclusion criteria
Exclusion criteria: 1. History of previous surgery of shoulder joint 2. Complete tear of rotator cuff muscles with complete atrophy 3. Uncontrolled systemic disease 4. Known hypersensitivity to any of the local anaesthetics drug under study 5. History of any platelet or coagulation related disease 6. Red Flag signs : fracture, fever, malignancy, infection, unexplained weight loss, numbness/weakness of upper limb, night sweats 7. Patients with human immunodeficiency virus (HIV,) hepatitis C virus (HCV) and hepatitis B virus (HBsAg)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the effect of platelet rich plasma (PRP) difference on shoulder pain and disability index (SPADI)Timepoint: 2 weeks, 1 month, 2 month, 3 month and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. change in analgesic requirement 2. change in range of shoulder movement 3. patient satisfaction score and platelet count 4. any side effectsTimepoint: 1.Baseline, 1 month, 2 month, 3 months, 6 months 2.Baseline, 1 month, 2 month, 3 months, 6 months 3. 3 months , 6 months 4. Baseline, 1 month, 2 month, 3 months, 6 months | — |
Countries
India
Contacts
Public ContactVanita Ahuja
Department of Anaesthesia and Intensive Care
Outcome results
None listed