Skip to content

study about postoperative analgesia after LSCS.

To compare the intrathecal hyperbaric Levobupivacaine with morphine verses hyperbaric Bupivacaine with morphine for postoperative analgesia after LSCS, a prospective randomised double blind study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/052067
Enrollment
80
Registered
2023-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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 Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Levobupivacaine with intrathecal morphine given at time of spinal anaesthesia before start of surgery: Primigravida term pregnant pt undergoing LSCS will be given Spinal anaesthesia: 1.

Sponsors

Sanjay Gandhi Post Graduate Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Term pregnant female Primary gravitational Singleton pregnancy Pfannenstiel incision ASA physical status 1 or 2

Exclusion criteria

Exclusion criteria: Patient refusal to participate ASA grade 3 or 4 Patient with coagulopathy, anatomical spine abnormalities, local infection in spine, pt who used anticoagulants or were unable to comprehend or use the verbal rating pain

Design outcomes

Primary

MeasureTime frame
To study the analgesics efficacy intrathecal heavy levobupivacaine with morphine Vs. heavy bupivacaine with morphine after caesarean section in term of time for first rescue analgesic demand. Timepoint: 0-4 hrs every 30 mins,4hrs,8hrs, 12 hrs, 16hrs,20hrs, 24hrs

Secondary

MeasureTime frame
To study the onset and duration of motor and sensory block. SAB related hypotension and cumulative vasopressor use and its effect on foetal PH. Pain assessment by NRS, on demand analgesic and total analgesic consumption. satisfaction score of pt and analgesic related side effects.Timepoint: 0-4 hrs every 30 mins,4hrs,8hrs, 12 hrs, 16hrs,20hrs, 24hrs

Countries

India

Contacts

Public ContactDr sandeep sahu

SGPGIMS lucknow

drsandeepsahu@yahoo.co.in8004904598

Outcome results

None listed

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