Skip to content

Clinical study on Habb-e-Asgand in the management of Rheumatoid Arthritis

To Evaluate the therapeutic efficacy of Habb-e-Asgand in the management of Waja-ul-Mafasil(Rheumatoid Arthritis).A Randomized, Single blind, Standard Controlled Trial.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039602
Enrollment
40
Registered
2022-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: M057- Rheumatoid arthritis with rheumatoid factor without organ or systems involvement

Interventions

Intervention1: Habb-e-Asgand (Pills): Ajwayin Desi(20g), Asgand(40g), Bidhara(40g), Bidhara(40g), Peepla Mool(20g), Pipal kalan(20g), Zanjabeel(40g), Satawar(40g), Musli siyah(20g) all are grounded to

Sponsors

Central Council for Research in Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Clinically diagnosed /or serological evidence of Rheumatoid arthritis(Waja-ul-Mafasil). 2 Patients who have agreed to sign the informed consent, follow the protocol and willing to participate in clinical trial voluntarily.3 Mild to Moderate cases of Rheumatoid Arthritis.4 Have a diagnosis of Rheumatoid Arthritis (RA) as defined by American College of Rheumatology/ European League Against Rheumatism (ACR/EULAR)2010 Criteria for the Classification of RA.

Exclusion criteria

Exclusion criteria: 1. Uncontrolled Diabetes mellitus. 2. Hepatic or Renal insufficiency. 3. Other type of arthritis. 4. Pregnancy and lactation. 5. Any joint surgery in the previous 6 months 6. Patients with cardiovascular diseases. 7. Patients who refuse to give the written consent for the study. 8. Severe cases of Rheumatoid Arthritis

Design outcomes

Primary

MeasureTime frame
Relief in signs and symptoms of Rheumatoid arthritisTimepoint: 45 days

Secondary

MeasureTime frame
Haematological, Radiological and Biochemical assessmentTimepoint: 45 days

Countries

India

Contacts

Public ContactDr Zaffar Hussain

Regional Research Institute of Unani Medicine, Srinagar

hussainzaffar6@gmail.com7006021996

Outcome results

None listed

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