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To find out whether low dose of Ketamine can provide effective and safe analgesia during labour.

Phase 2
Registration Number
CTRI/2008/091/000264
Lead Sponsor
nil
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
70
Inclusion Criteria

All parturient, with no antenatal risk factors and expected to have a normal vaginal delivery will be included in the study

Exclusion Criteria

Women with cardiac disease, gestational hypertension, epilepsy, known psychiatric disorder, multifetal pregnancy, cephalopelvic disproportion and previous caesarean section will be excluded from the study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the efficacy of low dose ketamine in providing obstetric analgesiaTimepoint: 10 point visual analogue scale
Secondary Outcome Measures
NameTimeMethod
To observe if this regimen has any side effects on the mother, the progress of labor and the fetusTimepoint: Mother- progress of labor,haemodynamic parameters, sedation, hallucinations and sleep disturbances. Baby- APGAR score at 1 and 5 minutes,the cord blood pH
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