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Effect of Unani formulations in knee ostioarthritis

Comparative clinical study on the efficacy of Habb-e-Mafasil with Roghan-e-Banafsha and Habb-e-Gul-e-Aakh with Roghan-e-Haft Barg in Waja'ur Rukbah (Knee Osteoarthritis)- A Randomized Clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070116
Enrollment
44
Registered
2024-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Habb-e- Mafasil,Roghan-e- Banafsha: Habb-e- Mafasil: 3 gm per day in two divided doses (2 pills of 750mg twice a day after meals) Roghan-e- Banafsha:10-15 ml per day Control Interventio

Sponsors

National Institute of Unani Medicine, Bengaluru
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Diagnosed cases of OA Knee Joint as per ACR Criteria16 (clinical, radiographical and laboratory). 2.Subjects of all genders aged 45-70 years. 3.Grade I and II of Kellgren Lawrence grading scale17

Exclusion criteria

Exclusion criteria: 1.Subjects who experience a rapid worsening of knee symptoms, have a hot swollen knee, have a previous knee replacement on the affected knee, have a history of significant trauma to the affected knee, have a joint injection or arthroscopy in the past 6 months, or have any major surgery in the last year. 2.Subjects currently taking, or in the past 3 months were taking, pain-relieving medications (e.g., nonsteroidal anti-inflammatory drugs, analgesics, and corticosteroids). 3.Subjects diagnosed with gout or pseudo gout within the last 3 months, have a history of gout in the knee joint, diagnosed with other inflammatory arthritis (e.g., rheumatoid arthritis, septic arthritis), and malignancy, diagnosed with a complex pain disorder or severe immobility (e.g., complex regional pain syndrome, severe back pain, multiple sclerosis, muscular dystrophy, Parkinson’s disease, or hemiplegia). 4.Participants with a recent diagnosis of, and/or currently suffering from uncontrolled medical conditions including but not limited to diabetes (RBS=180mg/dl), hypertension (=140/90mmHg), cardiovascular disease gall bladder disease/gallstones/biliary disease, endocrine disease, or malignancies. 5.Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Reduction in the total Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC –Modified CRD Pune version)Timepoint: 0th day, 7th day, 14th day, 21th day, and 28th day

Secondary

MeasureTime frame
1)Reduction in Pain intensity as per WOMAC (Modified CRD Pune version) pain scale 2)Reduction in stiffness as per WOMAC (Modified CRD Pune version) stiffness scale 3)Reduction in Restrictions of movements as per WOMAC (Modified CRD Pune version) physical activity scale Timepoint: 0th day, 7th day, 14th day, 21th day, & 28th day

Countries

India

Contacts

Public ContactDr Mohd Riyazuddin

National Institute of Unani Medicine

Shaikh.riyaz368@gmail.com8010392768

Outcome results

None listed

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