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Ayurvedic treatment for pain

Evaluation of analgesic and anti-infammatory activities of CONTRAPAIN -LEPA& OIL topical application in Musculoskeletal Disorders - CLINICAL STUDY

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/09/009907
Enrollment
80
Registered
2017-09-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- ï?µ Eighty (80) patients with MSD, meeting all inclusion/exclusion criteria will be included in the study

Interventions

Intervention1: Contrapain Lepa and Oil: Lepa powder contains drugs like Sigru, Punarnava, Kunduru, Rasna, Daruharidra, Shunthi, Lodhra, Devadaru,Nausadara, Chitraka, Sphatika Oil contains NirgundiPat

Sponsors

MB Life Scienes Pvt Ltd New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with musculoskeletal pain and swelling, fulfilling the diagnostic criteria of MS, willing to give consent for participating in the study. Patients who are currently on analgesics/NSAID, will be given a washout period of 7days prior to recruitment

Exclusion criteria

Exclusion criteria: Patients having severe MSD, those who are suffering from dermatitis or had a history of dermatitis, pregnant and lactating women, any other conditions which in the opinion of investigator will places the subject at risk or will influence the conduct of study or interpretation of results

Design outcomes

Primary

MeasureTime frame
Before and after the treatment period of 7 days Changes in following parameters between day 1 and day 7: â?¢ Subjective parameters: Pain (VAS), Tenderness, Shotha (swelling/Inflammation), Stabdata (Stiffness), Physician Global Assessment â?¢ Objective parameters: Range of Motion (Goniometer) At screening: RA, CRP, Serum Uric acid Safety Parameters: CBC, LFT, RFT (base line and 7th day) (Only 50% of Patients) Timepoint: Day 0, 8, 22,37

Secondary

MeasureTime frame
Assessment of subsidence after treatment period during the follow-up period up to 30 days. Subjective parameters will be assessed on day 15th and 30th day Timepoint: Day0, 8, 22 and 37

Countries

India

Contacts

Public ContactDrPradeep L Grampurohit

KLEUs Shri BMK Ayurveda Mahavidyalaya, Belagavi

pradeepgrampurohit@gmail.com9964144197

Outcome results

None listed

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