This study will be conducted for seeing the effect of a treatment where medicated decoction will be poured over the forehead as well as the whole body along with bandaging after application of paste of various medicinal powders with salt on patients with spastic cerebral palsy.
Phase 2
- Conditions
- Health Condition 1: F82- Specific developmental disorder ofmotor function
- Registration Number
- CTRI/2019/10/021730
- Lead Sponsor
- Sri Dharmasthala Manjunatheshwara College of Ayurveda and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
parents who are willing to sign consent form
if there was history of epilepsy and well controlled by medication
Exclusion Criteria
subjects with serious diseases like Tuberculosis meningitis encephalitis
subjects with poor controlled epilepsy juvenile DM complex seizures severe cognitive impairment and other genetic diseases will be excluded
severe handicap and deformities resulted from ling standing spasticity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessment criteria <br/ ><br>Goniometric measurements of affected joints <br/ ><br>Power of affected limbs <br/ ><br>Modified Ashworth scale of Spasticity <br/ ><br> <br/ ><br>Timepoint: Assessment is done on baseline treatment 15th 30th 45th 60th 75th and 90th day
- Secondary Outcome Measures
Name Time Method Assessment criteria <br/ ><br>Goniometric measurements of affected joints <br/ ><br>Power of affected limbs <br/ ><br>Modified Ashworth scale of SpasticityTimepoint: at 90th day