A clinical Study comparing the effectiveness of Simhnad Guggulu and Panchamrita Lauha Guggulu with Amalakadi Choorna in Manyastabha treatment.

Not yet recruiting

• Conditions: Spondylosis, unspecified. Ayurveda Condition: MANYASTAMBAH,

• Registration Number: CTRI/2025/05/087551
• Lead Sponsor: Dr Kuldeep Associate Professor Department of Kayachikitsa

Brief Summary

The present study is an interventional, open label, parallel group trial which aims to evaluate and compare the efficacy of Simhanad Guggulu and Panchamrita lauha guggulu along with Amalakadi choornam in the management of  manyastambha. One hundred and forty patient aged 20 - 60 years with classical features of mayastambha will be randomly categoriesd in two groups i.e 70 patients in each groups. In both groups for amapachana Amalakadi Choornam  will be given for 5 days which is followed by simhanad Guggulu 500mg  BD  in  Group A for 60 days. while in Group B after Amapachan Panchamrita lauha Guggulu 500mg BD for 60 days will be given.for both groups Ashtavargam Kashyam 30 ml is used as anupana for guggulu kalpas.After medication patient will  observed  for  30 days in both groups.  So overall study duration becomes 95 days and  followup will be done after 15 days .

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2025-05-23
• Study Start: 2025-10-06

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

• Subjects between the age group of 20 to 60 years.
• The subjects with classical signs and symptoms of Manyasthamba .
• Subjects of all genders, irrespective of religion and caste.

Exclusion Criteria

• Patients below 20 and above 60 years of age.
• Pregnant and lactating mother.
• Subjects with other systemic disorders such as accelerated hypertension, uncontrolled diabetes, gastritis, acid peptic disorder, hypothyroidism that interfere in the line of treatment.
• Subjects with congenital deformity, traumatic injuries, cervical stenosis & myelopathy, ankylosing spondylitis, infections of bones, and gross bony deformity.
• Patient suffering from autoimmune joint disorders.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction in Ruk(Pain), Stambha(Stiffness) of Manyapradesha.	95days

Secondary Outcome Measures

Name	Time	Method
Improvement in pain Vas Score, Neck disability index score and Neck range of movement	95 days

Trial Locations

Locations (1)

Shiva Ayurvedic Medical College and Hospital; 🇮🇳 Bilaspur, HIMACHAL PRADESH, India

Shiva Ayurvedic Medical College and Hospital

🇮🇳Bilaspur, HIMACHAL PRADESH, India

Dr Kuldeep

Principal investigator

7018918260

kdeep.thakur1990@gmail.com