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Effect of Roghan e suranjan over shoulder joint pain

Efficacy of Dalk-i-Layyin KathÄ«r with Roghan-i-SÅ«ranjÄ?n in the management of Wajaʹul Katif (Frozen Shoulder) - A Randomized Controlled Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/06/043494
Enrollment
26
Registered
2022-06-27
Start date
Unknown
Completion date
Unknown
Last updated
2022-08-02

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

Conditions

Health Condition 1: - Health Condition 2: M958- Other specified acquired deformities of musculoskeletal system

Interventions

Intervention1: Roghan-i-SÅ«ranjÄ?n: Patients of test group will be subjected to Dalk-i-Layyin KathÄ«r with Roghan-i-SÅ«ranjÄ?n. The intervention of Dalk-i-Layyin KathÄ«r will be started at first day

Sponsors

National Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Clinically diagnosed patients of frozen shoulder 2.Age more than or equal to 18 years 3.Either gender 4.Symptoms of frozen Shoulder that had lasted for at least 3 months. 5.Willing and able to provide informed consent

Exclusion criteria

Exclusion criteria: 1.Pregnancy and lactation 2.Previous manipulation of the affected shoulder under anesthesia in the last year 3.H/O the used of local corticosteroid inj. to the affected shoulder within the last 4 weeks or current corticosteroid therapy 4.uncontrolled DM (RBS >200mg/dl) 5.Other form of arthritis involving the shoulder (Rheumatoid arthritis, psoriatic arthritis, ankylosing arthritis) 6.Fracture or dislocation of the affected shoulder. 7.Previous shoulder surgery 8.Neurologic deficits affecting shoulder function 9 .Concomitant skin disease at the application site 10.History of allergy to lidocaine 11.Active non-controlled mental disorder 12.Multiple complete tears in ligament of rotator cuff 13.Any infection like COVID-19

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale (VAS)Timepoint: 0th day and 14th day

Secondary

MeasureTime frame
Improvement in Assesment ParametersTimepoint: two week

Countries

India

Contacts

Public ContactDr Mohd Nayab

National Institute of Unani Medicine

naheedmomin999@gmail.com9975148908

Outcome results

None listed

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