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se Of Bupivacaine With Fentanyl And Bupivacaine With Dexmedetomidine For Painless Labour

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2019/02/017456
Lead Sponsor
Indira Gandhi 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

1.ASA Physical status I or II parturients in active lobour with cervical dilatation of more than 3 cm.

2. Having full term live fetus without any obstetric complications.

3. Requesting epidural anagesia.

Exclusion Criteria

1. Body Mass index > 30.

2. Parturient Height < 150cm.

3. Age < 20 Years.

4. Anticipated difficult intubation.

5. Any contraindication for epidural catheter placement.

6. Sensitivity to study drug.

7. Administration of IV analgesics within 1 hour epidural request.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Study effect of epidural Bupivacaine and Fentanyl versus epidural Bupivacaine and Dexmeditomidine on Fetal outcome.Timepoint: From administration of drug to 12 hours after delivery of Baby outcome.
Secondary Outcome Measures
NameTimeMethod
To compare incidence of respiratory depression, Nausia- vomiting between patient receiving Fentanyl and dexmeditomidineTimepoint: From administration of drug to 12 hours after delivery of Baby.;To study effect of drugs on maternal hemodynamics in both groupsTimepoint: From administration of drug to 12 hours after delivery of Baby;To study VAS score in both groupsTimepoint: From administration of drug to 12 hours after delivery of Baby
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