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Effect of Unani Formulation and ibubrofen in the treatment of Osteoarthritis

CLINICAL EVALUATION OF A UNANI FORMULATION IN THE TREATMENT OF OSTEOARTHRITIS WITH SPECIAL REFERENCE TO EVALUATION OF ITS ANTIOXIDANT ACTIVITY

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2010/091/000585
Enrollment
60
Registered
2010-11-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Unani Formulation: Tablets (UNIM-301) Orally Twice Daily. Oil (UNIM-304) Used For Local Application UNIM-302(Pashoya) Used For Hot Fomentation On The Affected Joints Control Interventi

Sponsors

Central council for research in Unani medicine-CCRUM
Lead Sponsor
Central council for research in Unani medicine-CCRUM
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Aged between 40 to 70 years Either Sex Patients diagnosed according to American College of Rheumatology Criteria for osteoarthritis of different joints will be selected Patients with symptoms consistent with osteoarthritis of the joint involved for at least six months prior to screening. Patients, who will be willing to discontinue all NSAIDs or other analgesic medication taken for any condition, will be included in the test group. Willingness to sign the informed consent, follow the protocol and participate in clinical trial voluntarily.

Exclusion criteria

Exclusion criteria: Pregnancy and Lactation Diabetes mellitus Renal dysfunction Liver diseases Gastrointestinal diseases(Peptic ulcer disease) Other types of arthritis IHD and hypertension History of surgery of the joint involved Patients who will be unable to read/or understand the WOMAC questionnaire form

Design outcomes

Primary

MeasureTime frame
Clinical Parameters WOMAC Osteoarthritis Index Visual Analogue Scale (VAS) Active Range Of Motion (AROM)Timepoint: 1

Secondary

MeasureTime frame
hese Parameters Will Be Done Before The Treatment And After The Completion Of The Study Lipidperoxidation Reduced Glutathione Superoxide Dismutase Catalase Radiological Parameters X Rays Of The Affected Joints Will Be Taken Before And After Treatment To Compare Radiological Changes (If Any)Timepoint: 2

Countries

India

Contacts

Public ContactDr.M.Akhtar Siddiqui
drmasjh@rediffmail.com01126059686,9891273627

Outcome results

None listed

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