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ACTIVE NOT RECRUITING
NCT05279118
PHASE2/PHASE3

Ketogenic Diet vs ACTH for the Treatment of Children With West Syndrome

Sponsor: All India Institute of Medical Sciences

View on ClinicalTrials.gov

Summary

Children with West syndrome are prone to refractory seizures with poor neurocognitive outcome overall. The current standard of care consists of treatment with ACTH, but the grade of evidence is not high and not much RCTs are available. Ketogenic diet is an effective and well tolerated treatment option in drug refractory epilepsy and also in refractory west syndrome. In view of minimal side effects, better cost parameters and ability to continue for a longer duration our study aiims to investigate the efficacy of ketogenic diet as a first line therapy in comparison to ACTH therapy. Children with west syndrome after satisfying the inclusion and exclusion criteria will be randomised into the two treatment arms and primary response will be noted at the end of 6 weeks of therapy in terms of mean percentage of spasm reduction.

Official title: Comparison of Efficacy of Ketogenic Diet and ACTH Therapy Among Children With West Syndrome: A Pilot Randomized Control Trial

Key Details

Gender

All

Age Range

6 Months - 2 Years

Study Type

INTERVENTIONAL

Enrollment

80

Start Date

2022-04-18

Completion Date

2024-07-28

Last Updated

2024-06-25

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

Ketogenic diet

Children who have consented to the study and have been randomised to ketogenic diet arm will get ketogenic diet under supervision while starting with rapid hiking of lipid to carbohydrate ratio and primary response will be assessed at 6 weeks. Ketogenic diet ratio will be hiked quickly upto a maximum of 4:!. The duration of ketogenic diet can be extended beyond the period of study based on response and parental choice. A minimum period of 6 weeks of diet therapy will be undertaken baring any undue adverse effects when the primary outcome will be assessed

DRUG

ACTH

ACTH is the current standard therapy for children with west syndrome. Those who have been randomised to this arm will be started on high dose ACTH for 2 weeks followed by gradual tapering over remaining 4 weeks and primary response documented at 6 weeks of therapy. The high dose ACTh is 150U/m2 or 6U/kg dose administered IM daily for two weeks. After this the doses will be tapered gradually and ACTH will be stopped by 4 weeks for a total treatment duration of strictly 6 weeks.

Locations (2)

All India Institute of Medical Sciences

New Delhi, National Capital Territory of Delhi, India

AIIMS

New Delhi, India