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Comparison of Continuous Bupivacaine Wound Infiltration at Two Different Anatomical Planes for post Caesarean Analgesia - A Randomized Clinical Trial

Comparison of Continuous Bupivacaine Wound Infiltration at Two Different Anatomical Planes for post Caesarean Analgesia - A Randomized Clinical Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2016/07/007122
Enrollment
50
Registered
2016-07-26
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- 18 -35 years old primi gravida, at term pregnancy, ASA 1 or 2, posted for elective caesarean section under Spinal anaesthesia

Interventions

Intervention1: Continuous bupivacaine wound infiltration in the preperitoneal plane: Postoperatively at the incision site, wound infiltration catheter placed in the preperitoneal plane, i.e.,above the

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Primi gravida of 36 to 42 completed weeks of gestation, scheduled for elective caesarean section by Pfannenstiel incision ASA I and II

Exclusion criteria

Exclusion criteria: Spinal anaesthesia related problems such as failure to achieve adequate spinal level, perception of pain intraoperatively requiring opioid supplementation. Intraoperative surgical difficulties such as difficulty in closing peritoneum, excessive bleeding, uterine atony or operative injuries and placement of drain at wound site Any case of stillbirth or newborns requiring ICU care. History of allergy to local anaesthetics or NSAIDs. Any ongoing infection or sepsis Midline vertical skin incision Patient refusing spinal anesthesia

Design outcomes

Primary

MeasureTime frame
cumulative morphine consumptionTimepoint: 48 hours

Secondary

MeasureTime frame
Time interval till first PCA useTimepoint: within 48 hrs;Culture report of catheter flush sampleTimepoint: 48 hours;Duration of hospital stayTimepoint: Till discharge from hospital;Local wound discharge, bleeding â?? by inspection of woundTimepoint: 1 hr,2 hrs,3 hrs,4hrs, 5 hrs,6hrs, 12hrs,24 hrs,36 hrs,48 hrs;Pain at rest and at movement by VRSP scoreTimepoint: 1 hr,2 hrs,3 hrs,4hrs, 5 hrs,6hrs, 12hrs,24 hrs,36 hrs,48 hrs;Patient satisfactionTimepoint: 48 hours;Post operative nausea and vomiting, pruritus, sedationTimepoint: 1 hr,2 hrs,3 hrs,4hrs, 5 hrs,6hrs, 12hrs,24 hrs,36 hrs,48 hrs;Time interval before return of bowel movements, assessed from history regarding passage of first flatusTimepoint: within 48 hrs

Countries

India

Contacts

Public ContactDr Diana Thomas

Jawaharlal institute of postgraduate medical education and research

sakthiab8@gmail.com8903468132

Outcome results

None listed

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