Skip to content

Does local anaesthetic drug 0.08% levobupivacaine reduce the rate of instrumental vaginal delivery compared to another local anaesthetic drug 0.1% ropivacaine

Comparison of Epidural Boluses of 0.08% Levobupivacaine and 0.1% Ropivacaine Using Fentanyl as an Adjuvant for Labour Analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/01/011236
Enrollment
70
Registered
2018-01-10
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- pregnant patients

Interventions

Intervention1: 0.08% levobupivacaine with fentanyl: epidural catheter is inserted in patients with labour pain and analgesia is given by injecting 0.08% levobupivacaine with fentanyl via epidural cath

Sponsors

Mahatma Gandhi Medical College and Research Institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1) Primigravida with singleton pregnancy 2) Willing to involve in this study 3) Age between 18years to 30years. 4) Categorized under ASA PS I & II

Exclusion criteria

Exclusion criteria: 1)Patient refusal 2)High risk pregnancy 3)Primigravida with CPD 4)With fetal anomaly 5)Allergic to local anaesthetics 6)Injection site infection 7)Spine abnormalities 8)Significant coagulopathies.

Design outcomes

Primary

MeasureTime frame
Mode of delivery Timepoint: time of delivery

Secondary

MeasureTime frame
1. Hemodynamic ( SpO2, MAP, PR, FHR) 2. Foetal outcome 3. Maternal satisfaction 4. Side-effects.Timepoint: 1. every 10 minutes from initiation analgesia to delivery 2. 1 minute and 5 minute after baby delivery 3. 1 hour after baby delivery 4.from the initiation of analgesia to delivery of baby

Countries

India

Contacts

Public ContactAnnie Sheeba J

Mahatma Gandhi Medical College and Research Institute

annie.john24@yahoo.co.in9655035791

Outcome results

None listed

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