Skip to content

Comparing Marma Chikitsa and Cupping Therapy for Relieving Low Back Pain: A Clinical Study in Adults"

An Open Label Randomised Clinical Trial to Compare the Efficacy of Marma Chikitsa and Cupping Therapy in Management of Katigraha with Special Reference to Non-Specific Low Back Pain. - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/02/081194
Enrollment
90
Registered
2025-02-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: M545- Low back pain

Interventions

None listed

Sponsors

National Institute of Ayurveda
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with clinical findings suggestive of Katigraha (Non-specific low back pain) will be the potential trial subjects. Anatomical area - Pain between bottom of ribs and buttock creases. Age- Patients in the age group 21-50 years of either sex. Study specific criteria- Patients associated with only non-specific low back pain due to mechanical causes like low physical activity patients obese patients high physical stress at work. According to Oswestry Low Back Disability Questionnaire patients assessed with moderate score levels (15-24) of Non-specific low back pain. According to Back pain visual analogue scales (VAS) patients assessed with moderate score levels (4-6) of non- specific low back pain. Being provided with the details of this trial, understanding the details completely willingness to voluntarily participate and willingness to provide informed written consent upon detailed description of the study.

Exclusion criteria

Exclusion criteria: Patients suffering from any kind of major illness such as Rheumatoid arthritis or any other auto-immune diseases, Parkinsonism, paralysis, malignancy, severe anaemia, cardiac disease, HIV, Tuberculosis etc. According to Oswestry Low Back Disability Questionnaire patients assessed with mild (0-14) & severe (25-50)score levels of low back pain. According to Back pain visual analogue scales (VAS) patients assessed with mild (0-3) & severe (7-10) score levels of low back pain. Patients associated with Specific low back pain caused by an underlying disease (e.g., cancer), tissue damage (e.g., fracture), or may be referred from other organs (e.g., from kidney or aortic aneurysm). Pregnant women, Puerperal Period,Women during their Menstrual cycle duration. Patients on Hormonal therapies. Patients suffering from protrusion of lumbar disc and prolapsed inter vertebral disc. Patients suffering from low back pain related to high velocity trauma, fracture; or low back pain associated with severe or progressive neurological deficits. Patients who are dependent and not willing to taper psychoactive drugs (sedatives). Patients who are suffering from acute systemic illness. Patient who are suffering from fluctuating hypertension and diabetes. Patients having addiction (alcohol and narcotics). Judged inadequate by the investigators according to rejection and withdrawal criteria.

Design outcomes

Primary

MeasureTime frame
Change in intensity of symptoms of Katigraha as per Acharya Sodhal of Gadnigraha. Change in Intensity of symptoms of Non specific low back ache.Timepoint: 21 days

Secondary

MeasureTime frame
Change in grading level of Oswestry Low Back Disability Level & VAS Scale before and after the treatment.Timepoint: 21 days

Countries

India

Contacts

Public ContactDr Rashi Sharma

National Institute of Ayurveda, Deemed University, Jaipur, Rajasthan.

drskyadav4@gmail.com9413181445

Outcome results

None listed

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