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itrazepam versus Topiramate in Resistant Infantile Spasms

Phase 3
Conditions
Health Condition 1: G404- Other generalized epilepsy and epileptic syndromes
Registration Number
CTRI/2023/06/053933
Lead Sponsor
Postgraduate Institute of Medical Education and Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Children should be fulfilling the diagnostic criteria of IESS (ILAE 2022)

2.Male or female, age range 6-30 months at enrollment.

3.Failed to achieve the cessation of epileptic spasms on two of three first-line therapies (ACTH, oral steroids, vigabatrin therapy) or failure to achieve the cessation of epileptic spasms on one of three first-line therapies (ACTH, oral steroids, vigabatrin therapy) when other two options were either not feasible or considered not suitable by treating neurologists or declined by parents.

4.Within six weeks of failing on hormonal therapy and/or vigabatrin therapy

Exclusion Criteria

1. Parents decline to participate in the study.

2. Known contraindications for topiramate or nitrazepam (glaucoma, renal stone, liver disease)

3. Known allergy to topiramate or nitrazepam.

4. Co-intervention with another anti-seizure medication (ASM) in the last two weeks

5.Proven or suspected cases of neurometabolic or neurodegenerative disorder

6.Known history of aspiration pneumonia in last 3 months

7.Weight below 3 kg

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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