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Comparing midazolam to stop seizures when given through muscle versus when given through nose.

Not Applicable
Conditions
Health Condition 1: G00-G99- Diseases of the nervous systemHealth Condition 2: G402- Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures
Registration Number
CTRI/2018/10/016023
Lead Sponsor
AIIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

All age groups patients with drug refractory epilepsy admitted in epilepsy monitoring unit for Video EEG , AIIMS New Delhi

Exclusion Criteria

1.Patients with chronic kidney and liver disease

2.Patients with shock, hypotension and known respiratory illness.

3. Acute precipitant of seizure was major trauma, hypoglycemia, cardiac arrest or heart rate less than 40 beats per minute.

4.Pregnant patients

5.Patients known allergic to midazolam.

6. Patients with known Coagulopathy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean time in minutes/seconds required to terminate clinical and electrical seizure activity as documented by video EEG after drug administrationTimepoint: Patients having focal seizures for duration more than 5 minutes or generalized seizures more than 2 minutes will be given intranasal or intravenous midazolam as per randomization in following mentioned dose
Secondary Outcome Measures
NameTimeMethod
1.Serious adverse events related to midazolam. <br/ ><br>2. Local side effects related to drug route . <br/ ><br>3. Any injury related to seizuresTimepoint: â?¢Patients having focal seizures for duration more than 5 minutes or generalized seizures more than 2 minutes will be given intranasal or intravenous midazolam as per randomization in following mentioned dose
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