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Comparison Of Therapeutic Effect Of Jalaukavcharan And Cupping Therapy In Knee Pain

A Comparative Random Clinical Trial To Compare Efficacy Of Jalaukavcharan With Cupping Therapy In The Management Of Janu Sandhivata W.S.R.To Osteoarthritis Of Knee Joint - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/070194
Enrollment
60
Registered
2024-07-08
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: M170- Bilateral primary osteoarthritis of knee

Interventions

None listed

Sponsors

Institute For Ayurved Studies And Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient Having Sign And Symptoms Of Second Degree/Grade Osteoarthritis Of Knee Joint As Explained In Modern Text Books And Ayurvedic Text Books Related To The Topic. Patient Between The Age Of 35-70 Years. Patients Of Both Sex. Patients Who Will Be Willing For The Treatment.

Exclusion criteria

Exclusion criteria: 1. Blood Clotting Disorder. 2. Allergic Reaction To Active Substances Of The Leech. 3. Pregnant Women. 4. Secondary Osteoarthrithis (Amavata And Vatarakta Etc.). 5. Patient With Condition Mentioned Under Contraindication For Jalaukavcharan in Sushruta Samhita and Cupping Therapy. 6. Patients With Systemic Diseases Like Uncontrolled Diabetes,Uncontrolled Hypertension,Patients With Major Disorder Like Neoplastic Conditions Of Knee. 7. T.B.Knee Joint. 8. Patient With Condition Haemarthrosis Pyoarthorosis. 9. Patient Undergoing Other Modalities Of Treatment For Janu Sandhivata.

Design outcomes

Primary

MeasureTime frame
To give relief in pain, stiffness, tenderness, restrictions of motion,swelling,crepitus to osteoarthritic patient. To increase their quality of life . Timepoint: Assessment of outcome on -baseline (0th day ),1st week(7th day),2nd week(14th day),3rd week(21th day),4th week(28th day) Treatment Duration of Study–21 Days( On 0th,7th,14th,21th Day) Follow Up– Follow Up On 28th 35th 49th day.

Secondary

MeasureTime frame
OBJECTIVE CRITERIA :-Stiffness, Restriction of flexsion of knee joint . SUBJECTIVE CRITERIA :- Pain , Tenderness , Swelling , Crepitus.Timepoint: Outcome assessed- On baseline 0th day),1st week(7th day),2nd week(14th day),4th week(21th Day(. Follow Up–Four Follow Up On 28th 35th 49th day.

Countries

India

Contacts

Public ContactSudesh

Institute For Ayurved Studies And Research

sudeshkumari1712@gmail.com09466605830

Outcome results

None listed

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