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Peechu(enema)with otradam(fomentation) for Mulangaal Vatham(osteoarthrits)

An Open,Non Randomised Single Arm Single centric Clinical Trial to determine the Therapeutic effectiveness of Peechu Thearapy(medicated enema) & Mulangaal Vatha Otradam (Fomentation) in the management of Azhal Keelvayu (osteoarthritis) - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054601
Enrollment
30
Registered
2023-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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: Peechu and otradam: Peechu for 3 days Rest for 1 day Otradam for 6 days Control Intervention1: Nil: Nil

Sponsors

National Institute of Siddha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: A] Patients who will be fulfill any of the following criteria will be included in the Age: 30- 70Yrs Sex – Both male and female B] Patients who will be having classical symptoms of pain &swelling of knee joints, stiffness & restricted movements. C] X-ray knee joint showing osteoarthritis D] Willing to give blood samples before and after treatment. E] Patient willing to sign the informed consent stating that he/she will conscientiously stick to the treatment during 10 days but can opt out of the trial of his/her own conscious discretion. F] Patients who are willing to take radiological investigations. Patient having clinical symptoms of difficulty in walking, stiffness, tenderness in knee Joint

Exclusion criteria

Exclusion criteria: Rheumatoid arthritis Gouty arthritis Tubercular arthritis Any other serious systemic illness Cardiac disease Chronic kidney disease Liver diseases Intestinal disease Having piles and fistula Patient not willing for peechu therapy

Design outcomes

Primary

MeasureTime frame
The reduction in pain & restricted movements which was measured using goniometer & spadi indexTimepoint: 12 months

Secondary

MeasureTime frame
NilTimepoint: Nil

Countries

India

Contacts

Public ContactDr DPeriyasami

NATIONAL INSTITUTE OF SIDDHA

sami2011nis@gmail.com7358481734

Outcome results

None listed

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