A clinical trial to study the effect of the drug lekhaniya mahakashaya on patients of obesity(hyperlipidemia)
- Conditions
- Patient of sthaulya (Hyperlipidemia)
- Registration Number
- CTRI/2018/02/011874
- Lead Sponsor
- Ch brahm prakash ayurved charak sansthan khera dabar najafgargh
- Brief Summary
Obesity is a prevalent nutritional disorder in which energy intake exceeds the energy output over a sufficiently long period of time and energy stores of the body remain too large, although the genetic component to obesity remains a possibility, it is unlikely to be great or to prevent weight loss being possible in most patient by reducing energy intake. environmental influences are believed to be more important in explaining the familial association in obesity.An inactive lifestyle is thought to play a role in the development of obesity.
**Drugs-**Lekhaniya mahakashaya
**Dose-** 48 gm BD with luke warm water
**Study type**-Interventional
**Study time-**18 Months
**Interventional time**-40 Days
**Sample size**-20 Patient in each group
**Group1**- Lekhaniya mahakashaya kwath
**Group2-** pathya ahar vihar and yoga asan and exerscise
**Assessment criteria-**
**Subjective criteria-** chal sphik, utsaha hani,ksudra swas,atinidra,swedadhikya,anga daurgandhya,anga gauravata,ati pipasa,ati ksuda
**Objective criteria-** chest, abdomen, hip, mid thigh, mid arm, BMI range (kg/m2)
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 40
- The well diagnostic pt.of sthaulya (Hyperlipidemia)will be selected s.cholesterol->200mg/dl s.
- triglyceride- > 150mg/dl s.LDL- >110 S.VLDL-> 40mg/dl.
- suffering with any systemic disease like cardiac and renal disease hypertention.
- pt suffering for endocrine disorder like diabetes thyroid dysfunction etc.
- pregnant females and lactating females.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Reduce symptoms of obesity and relief of symtoms 18 month like atinidra,chala sphik,utsaha hani,kshudra shawas anga daurgandhya etc 18 month
- Secondary Outcome Measures
Name Time Method 1.aetiopathogenesis of sthaulya will be assessed by adopting suitable subjective parameters. 2.Decrease elevated level of s.cholesterol s.triglyceride s. LDL S.VLDL Etc.
Trial Locations
- Locations (1)
Ch brahm prakash ayurved charak sansthan khera dabar najafgarh 73
🇮🇳Delhi, DELHI, India
Ch brahm prakash ayurved charak sansthan khera dabar najafgarh 73🇮🇳Delhi, DELHI, IndiaProf Dr Vidula GujjarwarPrincipal investigator9990174348shreemahalaxmi1969@gmail.com