Comparison of levobupivacaine and levobupivacaine with fentanyl for spinal anesthesia in lower belly surgeries

Prospective Randomised Comparative Study of Intrathecal Levobupivacaine and Levobupivacaine with Fentanyl in Infraumbilical Surgeries - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/04/084688

Enrollment

Registered

2025-04-13

Start date

Unknown

Completion date

Unknown

Last updated

2025-04-28

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: Intrathecal Levobupivacaine 0.75% Hyperbaric: Dose : 22.5mg (3ml) Route: Intrathecal Duration : Bolus over 10 seconds Frequency : single dose Control Intervention1: Intrathecal Administ

Eligibility

Inclusion criteria

Inclusion criteria: All patient giving consent undergoing infraumbilical surgeries ASA grade I,II

Exclusion criteria

Exclusion criteria: Patients known or suspected to have allergy for study drug. Patients with any infection at the site of injection Pregnant patients

Design outcomes

Primary

Measure	Time frame
The primary objectives is to compare the onset and duration of sensory and motor block in subarachinoid block given with levobupivacaine versus levobupivacaine with fentanylTimepoint: baseline , after intrathecal administration of drug at 2 mins , 4 mins, 6mins,8mins,10mins,12mins,14mins,16mins,18mins,20mins and 30mins	—

Secondary

Measure	Time frame
Hemodynamic changes between two groups including hear rate , blood pressure and mean arterial pressureTimepoint: baseline , after induction at 2 mins , 4 mins, 6mins,8mins,10mins,12mins,14mins,16mins,18mins,20mins and 30mins	—

Countries

India

Contacts

Public ContactDr Rochana Bakhshi

D Y Patil Hospital

drrochana@yahoo.com9323272151

Outcome results

None listed

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