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A clinical trial to study effect of shunthyadi churna in drooling in children with cerebral palsy

Evaluation of Shunthyadi churna in management of drooling in children with cerebral palsy –a randomised controlled clinical trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/09/074359
Enrollment
30
Registered
2024-09-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G809- Cerebral palsy, unspecified

Interventions

None listed

Sponsors

DR SAKSHI GANDHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex in age group between 4years-16 years Patients fulfilling the diagnostic criteria will be included for the study Children who have not received any form of modern intervention for drooling at least in last 3 months Children who have previous MRI report which is suggestive of diagnosis of cerebral palsy(HIE Periventricular leukomalacia etc)

Exclusion criteria

Exclusion criteria: Use of drugs that interfere with salivation study outcome(anticholinergic and neuroleptic drugs like atropine benzhexol hydrochloride etc) Patients with any known congenital anomalies like Congenital Heart Disease (CHD) cleft lip cleft palate etc will be excluded Patients with other disease status like Acute infections, severe systemic illness and children with any progressive neurologic anomalies will be excluded from the study. Children with any local ulcerations wounds etc in oral cavity will be exclude MRI report suggestive of any other brain tissue damage leading to drooling other than cerebral palsy (Congenital malformation Bleeding traumatic brain injury etc) MRI report of more than 1 year old

Design outcomes

Primary

MeasureTime frame
There might be significant effect of shunthyadi churna in the management of drooling in children with Cerebral Palsy Primary outcome –Measured by changes in Drooling Impact Scale Timepoint: 0 day 7th day 15th day

Secondary

MeasureTime frame
Modified Teachers drooling Scale Quality of life of Cerebral palsyTimepoint: 0 day 7th day 15th day

Countries

India

Contacts

Public ContactDr AZIZAHMED I ARBAR

Department of Kaumarabhritya KLE Shri BMK Ayurveda Mahavidyalaya Shahapur Belagavi

azizarbar@gmail.com9844532113

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026