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Clinical Trials/CTRI/2025/11/096832
CTRI/2025/11/096832Not yet recruitingPhase 3

A COMPARATIVE CLINICAL STUDY TO EVALUATE THE EFFICACY OF BHAVAPRAKASHOKTA SHEPHALIKA PATRA KASHAYAM AND RASNA GUGGULU IN GRIDHRASI W.S.R. TO SCIATICA

Govt ayurveda college nipaniya rewa mp1 site in 1 country40 target enrollmentStarted: April 30, 2026Last updated:

Trial Snapshot

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Enrollment
40
Locations
1
Primary Endpoint
improvement in subjective parameters like Ruk Stambh Tod Muhuspandana Graha Aruchi Tandra Gaurava

Study Overview

Brief Summary

The present clinical study entitled A Comparative Clinical Study to Evaluate the Efficacy of Bhavaprakashokta Shephalika Patra Kashayam and Rasna Guggulu in Gridhrasi w.s.r. to Sciatica aims to evaluate and compare the therapeutic effects of two classical Ayurvedic formulations in the management of Gridhrasi, a Vatavyadhi closely correlated with sciatica.

Gridhrasi is characterized by  Ruka   Stambha Toda Muhuspandanaand  Sakthikshepa Nigrahaoften accompanied by Tandra, Gaurava, and Arochaka in Kaphanubandha type. The condition corresponds to the modern entity “sciatica,” involving radiating pain along the sciatic nerve due to compression or irritation.

The study is designed as a prospective, open-labelled, randomized clinical trial conducted on 40 patients, divided into two groups of 20 each.

Group A Shephalika Patra Kashayam   50 ml twice daily before meals

Group BRasna Guggulu   250 mg twice daily after meals

The treatment duration is 30 days, with a follow-up of 15 days, and both groups receive Ushna Jala as Anupana.

Both formulations are selected for their Vata-Kapha Shamak, Vedanasthapana, Amapachaka, and Shothahara properties.

Shephalika Patra Kashayam *Vitex negundo Linn.*possesses Ushna Veerya and Katu Vipaka, aiding in pain and inflammation reduction and Amapachana.

Rasna Guggulu combines Rasna Pluchea lanceolataand Guggulu  Commiphora mukul providing potent Vatashamaka, anti-inflammatory, and analgesic actions.

This study seeks to establish a comparative evaluation of these two Ayurvedic regimens to determine which provides better relief in terms of pain, stiffness, and functional improvement, thereby offering an effective, safe, and economical alternative for the management of Gridhrasi

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
16.00 Year(s) to 70.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Patients aged between 16 to 70 years of any gender 2.Patients having clinical signs and symptoms of Gridhrasi 3.Patients willing to sign the informed consent form
  • SLR (Straitght Leg Raising) Test positive.

Exclusion Criteria

  • Pregnancy & Lactating women
  • Tuberculosis of spine
  • Diabetes mellitus
  • Cardiac Disease
  • Congenital Disease
  • Traumatic injury.

Outcomes

Primary Outcomes

improvement in subjective parameters like Ruk Stambh Tod Muhuspandana Graha Aruchi Tandra Gaurava

Time Frame: on 0 days to 30 days

Secondary Outcomes

  • improvement in subjective parameters like Ruk Stambh Tod Muhuspandana Graha Aruchi(on 0 days to 30 days)

Investigators

Sponsor
Govt ayurveda college nipaniya rewa mp
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Jitendra Patel

Govt ayurveda college nipaniya rewa mp

Study Sites (1)

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