Comparision of Epidural Fentanyl to Epidural Dexmedetomidine on Requirement of Ropivacaine Dose in Patient Controlled Pain relief with epidural During Delivery
Not Applicable
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated deliveryHealth Condition 2: 1- Obstetrics
- Registration Number
- CTRI/2024/07/069716
- Lead Sponsor
- Vijayanagar 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 Full term parturients with 37 weeks or greater period of gestation, both primi and multigravida.
2 Singleton pregnancy with vertex presentation.
3 Inactive phase of labour cervical dialation 3 to 4 cms
4 Age more than 20years
5 ASA-2
6 Willing to give consent for labour epidural analgesia
7 Parturient who can understand and able to use PCA pump
Exclusion Criteria
1.Allergy to any of the study drugs
2.Patients with history of significant disorders (Pregnancy induced hypertension, diabetes mellitus, obstetric haemorrhage, other cardiovascular, respiratory, central nervous system or renal system disorders)
3.Significant coagulopathy
4.Other contraindications: localized sepsis, raised ICP etc.
5.Previous LSCS
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Consumption of Total Dose of Ropivacaine 0.1% in Both the Groups by Patient Controlled Epidural Analgesia in LabourTimepoint: From 4cm Cervical Dilatation till the End of Stage 3 of Labour
- Secondary Outcome Measures
Name Time Method