A clinial trial to study analgesic effect of two drug Inj. Ropivacine and Inj. Levobupivacaine via epidural analgesia for labour pain relief.

Analgesic efficacy of Epidural Ropivacaine versus Epidural Levobupivacaine with fentanyl as adjuvant during second stage of labour : A Comparative study - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/069689

Enrollment

128

Registered

2024-06-28

Start date

Unknown

Completion date

Unknown

Last updated

2024-07-22

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Epidural Analgesia: Epidural catheter inserted as per standard protocol at 4 cm of cervical dilatation Control Intervention1: Epidural Levobupivacaine: Inj Levobupivacaine 0.1% with Inj

Eligibility

Inclusion criteria

Inclusion criteria: Primigravida requesting for labour analgesia Full term (37-42 weeks) pregnancy Live singlton pregnancy Cephelic presentation

Exclusion criteria

Exclusion criteria: ASA Grade III & IV History of opioid use Recived MgSO4 Recived oral or intravenous analgesia during labour Cervical dilatation of 4 cm or more at epidural request Contraindictaion to epidural analgesia Containdication to vaginal delivery

Design outcomes

Primary

Measure	Time frame
Maternal analgesia using VAS scoreTimepoint: VITALS PR BP SPO2 VAS score recoreded every 5 minutes for initial 15 minutes then every hour untill delivery	—

Secondary

Measure	Time frame
Duration of LabourTimepoint: after delivery;Maternal Satisfaction using Likert"s satisfaction scoreTimepoint: at the end of procedure;Mode of deliveryTimepoint: At the time of delivery;Moter block using Modified Bromage scoreTimepoint: recoreded every 5 minutes for initial 15 minutes then every hour untill delivery;Neonatal outcome using APGAR ScoreTimepoint: 1minute and 5 minutes after birth;side effects and complication (Hypotention , Epidural hematoma , Sever Headach)Timepoint: at the end of procedure	—

Measure

Time frame

Duration of LabourTimepoint: after delivery;Maternal Satisfaction using Likert"s satisfaction scoreTimepoint: at the end of procedure;Mode of deliveryTimepoint: At the time of delivery;Moter block using Modified Bromage scoreTimepoint: recoreded every 5 minutes for initial 15 minutes then every hour untill delivery;Neonatal outcome using APGAR ScoreTimepoint: 1minute and 5 minutes after birth;side effects and complication (Hypotention , Epidural hematoma , Sever Headach)Timepoint: at the end of procedure

—

Countries

India

Contacts

Public ContactDr Pooja Shakar

Pt JNM Medical College Raipur CG

jayalalwani2020@gmail.com9300224989

Outcome results

None listed

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