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Comparison of labor epidural with three different doses of fentanyl

Labor Epidural Analgesia: Comparison of intermittent boluses of ropivacaine with three different concentrations of fentanyl - A randomized control Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/07/026662
Enrollment
100
Registered
2020-07-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Epidural group with fentanyl 1�µg/ml: Parturient will receive 20ml of 0.1% ropivacaine with fentanyl 1�µg/ml Intervention2: Epidural group with 1.5 �µg/ml fentanyl: Will receive

Sponsors

Amrita Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consenting parturients of the American society of anaesthesiologists, grade1 and 2 having uncomplicated cephalic singleton pregnancy and desirous of having a labour epidural

Exclusion criteria

Exclusion criteria: Hypersensitivity to study drugs, bleeding disorders, decreased platelet counts, sepsis, spinal column deformities, history of spine surgery and if parturient delivers before administering the second bolus dose.

Design outcomes

Primary

MeasureTime frame
Assessment of duration of adequate analgesia with each bolusTimepoint: Till delivery of baby

Secondary

MeasureTime frame
onset of analgesia, incidence of sedation, pruritus, instrumental delivery, conversion to caesarean section and fetal outcomes like bradycardia, fetal acidosis and Apgar.Timepoint: Till delivery of baby

Countries

India

Contacts

Public ContactSajan

Amrita Institute of Medical Sciences

nituveesundeep@gmail.com09495962020

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026