A Clinical trial on Komoothira Silasathu Chooranam in the management of Thandagavatham (Lumbar spondylosis) among patients attending OPD and IPD of Government Siddha Medical College and Hospital,Palayamkottai
Phase 2
- Conditions
- Health Condition 1: M478- Other spondylosis
- Registration Number
- CTRI/2024/06/068547
- Lead Sponsor
- GOVERNMENT SIDDHA MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Pain and stiffness in the lumbar region
2.Patient presenting with or without radiating pain to lower limb
3.Difficulty in range of motion
4.Patient who are willing to participate in the study
Exclusion Criteria
1.Osteoarthritis of hip
2.Patient undergone spinal surgery
3.TB-Spine
4.SLE
5.Infection
6.Rheumatoid arthritis
7.Fracture of spine
8.Chronic renal and liver disease patients
9.Pregnancy and lactating mother
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The outcome will be aimed at reducing the symptoms of Thandagavatham(Lumbar sponsylosis)and to determine the therapeutic efficacy of clinical trials drug(komoothira silasathu chooranam)Timepoint: 48 days
- Secondary Outcome Measures
Name Time Method 1.To collect various aspects of Thandagavatham in Siddha literatures. <br/ ><br>2.To evaluate physico chemical,phyto chemical and bio chemical characters of Komoothira Silasathu chooranam. <br/ ><br>3. To evaluate safety profile for assessing acute and sub-acute toxicity of trial drug Komoothira Silasathu chooranam. <br/ ><br>4.To evaluate pharmacological analysis of Komoothira Silasathu chooranam. <br/ ><br>5.To Study about the prevalence of Thandagavatham in relation between diet and life style. <br/ ><br>6.To evaluate siddha parameters (including Envagai thervu) changes and dhegi of Thandagavatham patients during the study period. <br/ ><br>7. To evaluate modern parametric changes in Thandagavatham patients <br/ ><br>8.To document the Bio statistical analysis. <br/ ><br>9. To assess the Quality of life of Thandagavatham patients.Timepoint: 6 months