To study the efficacy and safety of injectable paracetamol with injectable tramadol in labor
Phase 4
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2023/09/057683
- Lead Sponsor
- SIKKIM MANIPAL INSTITUTE OF MEDICAL SCIENCES
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Consenting women in early/active phase of labour at =37weeks gestation
Singleton pregnancy with cephalic presentation
Exclusion Criteria
Multiple Pregnancy and mal-presentation
Intrauterine fetal death
Women who do not consent for the study.
<37 weeks period of gestation
History of allergy to any of the study drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To check the efficacy of intravenous paracetamol with intramuscular tramadol when used as labor analgesicsTimepoint: 10 mins <br/ ><br>30mins <br/ ><br>1 hourly after the administration of drug
- Secondary Outcome Measures
Name Time Method To check the safety of injection paracetamol with injection tramadol when used as labor analgesicsTimepoint: 0hrs to 24 hrs after delivery