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Prospective study of labour analgesia with low dose of ketamine - obsevational study

Phase 4
Conditions
Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Registration Number
CTRI/2022/12/048014
Lead Sponsor
AARUPADAI VEEDU MEDICAL COLLGE
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

metioned above

Exclusion Criteria

only 18 to 30 years remaning all excluded

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
ketamine is very effective and providing anaglgesiaTimepoint: BEFORE LABOUR 3 HOURS TO AFTER DELIVERY 5 HOURS I WILL MONITOR
Secondary Outcome Measures
NameTimeMethod
TO REDUCE LOBOR PAINTimepoint: 24HRS
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