CTRI/2018/03/012384
Completed
Phase 4
A study comparing the efficacy of two techniques,PIEB and PCEA on the consumption of epidural levobupivacaine and fentanyl mixture in labouring parturients.
Government Medical College and Hospital Chandigarh0 sites50 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- American Society of Anaesthesiologists (ASA) grade I and IIHealth Condition 2: O80- Encounter for full-term uncomplicated delivery
- Sponsor
- Government Medical College and Hospital Chandigarh
- Enrollment
- 50
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •American Society of Anaesthesiologists (ASA) grade I and II
- •Age \>18 years
- •Primigravida
- •Single gestation
- •Cephalic presentation at \>\= 36 weeks of gestation
- •In early spontaneous labour (cervical dilation \<\= 5 cm)
- •Baseline pain score \> 30 (on a 0\-100 VAS)
- •Able to use PCEA pump
- •Requesting epidural analgesia for labour
Exclusion Criteria
- •refusal by parturient
- •parturients who had received parentral opioids in last 4 hours
- •systemic and local sepsis
- •deranged coagulation profile
- •parturients having multiple pregnancies and premature labour
- •obstetric complications (premature rupture of amniotic membrane,antepartum haemorrhage, eclampsia)
- •chorioamnionitis
- •HELLP syndrome
- •noncephalic presentation
- •allergy to study drugs,i.e.,levobupivacaine and fentanyl
Outcomes
Primary Outcomes
Not specified
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