Normal delivery using epidural anaesthesia with total painless method

Effectiveness of bupivacaine and levobupivacaine for epidural labour analgesia - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/03/082474

Enrollment

Registered

2025-03-17

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

None listed

Interventions

Intervention1: Levobupivacaine plain: 19 G epidural catheter inserted at L4-L5 interspace under Local anaesthesia and Inj. Levobupivacaine 0.2% 12 ml as bolus via epidural catheter at the time of more

Eligibility

Inclusion criteria

Inclusion criteria: Full Term Female Pregnant Women Singleton Pregnancy and Vertx Presentation Active stage of labour ASA Grade I

Exclusion criteria

Exclusion criteria: Cardiovascular disease, Neuromuscular diseases Major sicknesses like bronchial asthma and tuberculosis Severe eclampsia Received opioid or sedative drugs Drug allergies Physical disability

Design outcomes

Primary

Measure	Time frame
To determine the overall effectiveness of levobupivacaine or ropivacaine in terms of onset,quality of analgesia and degree of motor blockadeTimepoint: To determine the overall effectiveness of levobupivacaine or ropivacaine in terms of onset,quality of analgesia and degree of motor blockade	—

Secondary

Measure	Time frame
To Assess the maternal fetal outcome & maternal satisfaction scoreTimepoint: at the time of delivery of the baby & thereafter every hour till 6 hrs after delivery	—

Countries

India

Contacts

Public ContactDr Brajesh Kaushal

Gandhi Medical College

brajeshkaushal3@gmail.com9425772151

Outcome results