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Clinical Trials/CTRI/2025/02/081151
CTRI/2025/02/081151Not yet recruitingPhase 2/3

A randomized comparative clinical study to determine the efficacy of vishwadi guggulu and rasna guggulu along with sahacharadi taila matra basti in gridhrasi

Dr Joylin Joshina Jathanna1 site in 1 country60 target enrollmentStarted: March 4, 2025Last updated:

Trial Snapshot

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Ruk/Pain

Study Overview

Brief Summary

It is a clinical study to evaluate the effectiveness of rasna guggulu and vishwadi guggulu with sahacharadi taila matra basti given in the patients of gridhrasi.Total 60 number of patients divided into 2 groups and administered with above drugs, internal medication for 30 days and matra basti for 15 days. Assessment parameters like ruk, toda, sthambha, spandana, aruchi, tandra, gourava as subjective parameters and SLR, bregards sign, 50 feet walk test as objective parameters are observed on 0th, 15th, 30th, 60th day at Kayachikitsa OPD, ALN rao memorial ayurvedic hospital.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
20.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Subjects of either sex 2.Subjects within the age group of 20 to 60 years
  • Subjects with clinical features of Gridhrasi such as ruk, toda, stambha, spandana which starts from sphik pradesha and radiating towards foot along with aruchi, tandra and gourava will be included 4.Chronicity less than 5 Years 5.Subjects with controlled systemic disorder such as Diabetes mellitus, Hypertension etc 6.Subjects must be capable of giving informed consent, willingness and ability to comply with scheduled visits, treatment plans and laboratory tests and other study procedures.

Exclusion Criteria

  • Pregnant and Lactating women
  • Subjects with diagnosed uncontrolled systemic disorder such as Diabetes mellitus, Hypertension, etc.
  • Gridhrasi due to any post-surgical complication,infective and degenerative conditions of spine.
  • 5.Patients with H/O acute traumatic injury.
  • (Complications of cauda equina syndrome).

Outcomes

Primary Outcomes

Ruk/Pain

Time Frame: 30 days

Toda/Pricking pain

Time Frame: 30 days

Stambha/Stiffness

Time Frame: 30 days

Spandana/Pulsating

Time Frame: 30 days

Aruchi/loss of taste

Time Frame: 30 days

Tandra/Drowsy

Time Frame: 30 days

Gourava/Heaviness

Time Frame: 30 days

Secondary Outcomes

  • not applicable(not applicable)

Investigators

Sponsor
Dr Joylin Joshina Jathanna
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Joylin Joshina Jathanna

ALN Rao Memorial Ayurvedic Medical College Koppa Chikmagalur

Study Sites (1)

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