A clinica trial on VISHNUKIRANTI KUDINEER in the management of CEGANAVADHAM (CERVICAL SPONDYLOSIS)
- Conditions
- Other spondylosis, (2) ICD-10 Condition: M478||Other spondylosis,
- Registration Number
- CTRI/2022/02/040374
- Lead Sponsor
- Government Siddha Medical College and Hospital
- Brief Summary
The study is a Prospective Open labelled phase II non randomized clinical study to evaluate the therapeutic efficacy of VISHNUKIRANTI KUDINEER in the management of CEGANAVADHAM(CERVICAL SPONDYLOSIS). The trial drug will be administered at the dose of 30-60 ml /twice a day (orally) 45 days in 40 patients. The trial period of 12 months will be carried out in Government Siddha Medical College and Hospital, Palayamkottai, Tirunelveli, Tamilnadu. The primary out come will be the evaluations of siddha diagnostic parameters, assessment of safety profile of trial drug, assessment of pharmacological and biochemical parameters of trial drug. In case of any adverse events (AE) noticed and it will be referred to pharmacovigilance department of SCRI. Further management of patients will be given in OPD facility
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 40
Neck pain radiating to upper limb with or without numbness, guiddiness and neck stiffness Restriction neck movememts Willing for doing laboratory investigation and xray imaging The neck diability index score should be equal or greater than 40%.
Age less than 20 greater than 60 Traumatic injury Systemic hyper tension Ischeamic heart diseases Chronic kidney disease Tuberculosis of spine Secondary maliganancy Chronic systemic illness Congenital spinal anomaly Pregnancy Lactating mother Extra cervical rib.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Reduction of the symptoms of painin neck and upper limbs 45 days Improvement of the range of movements in the neck and upper limbs 45 days The outcome is aimed at reducing pain and increasing the range of movements 45 days Good improvement-score 10%/below10% 45 days Moderate improvement-score10-20% 45 days Mild improvement-score 20-30% 45 days No improvement-score 40% 45 days
- Secondary Outcome Measures
Name Time Method To evaluate the physicochemocal, phytochemicals, biochemical analysis of clinical trial drug To evaluate the safety profile for acute and subacute toxicity of the trial drug
Trial Locations
- Locations (1)
Govt siddha medical college and hospital
🇮🇳Tirunelveli, TAMIL NADU, India
Govt siddha medical college and hospital🇮🇳Tirunelveli, TAMIL NADU, IndiaSarumathi SPrincipal investigator7639531129mugamathi53@gmail.com