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Portal Blocks for relief of postoperative pain in patients undergoing Cesarean section

Portal Blocks for relief of postoperative pain in patients undergoing Cesarean section, a one year non randomized trial - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062211
Enrollment
60
Registered
2024-02-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: O82- Encounter for cesarean delivery without indication

Interventions

Intervention1: Portal Block: Intervention group will receive portal block post operatively when NRS score is More than or equal to 7. Portal block consists of a single shot Injection of lignocaine 0.1

Sponsors

Dr Ravi Kerur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I and II. Age between 20 to 40 years. Weight ranging from 70-90kg Height ranging from 155-185cm (5ft to 6ft) Patients undergoing LSCS under spinal anesthesia Provides Consent

Exclusion criteria

Exclusion criteria: Patient who refuse to give consent. Patient with obstetric complications Patient with suspected fetal compromise Coagulopathy Patients who do not fulfill inclusion criteria.

Design outcomes

Primary

MeasureTime frame
To evaluate efficacy of portal blocks for post-operative pain management in woman undergoing Cesarean section using NRS scores for assessment of pain.Timepoint: At Baseline before administration of block, then 20 min after block then 1hr,2hr,3hr,4hr,5hr,6hr,24hr,48hr after the block

Secondary

MeasureTime frame
To Evaluate patient satisfaction, effects on hemodynamic parametersTimepoint: At Baseline before administration of block, then 20 min after block then 1hr,2hr,3hr,4hr,5hr,6hr,24hr,48hr after the block

Countries

India

Contacts

Public ContactDr Ravi Kerur

Jawaharlal Nehru Medical College, Belagavi

ravikerur@gmail.com7026380920

Outcome results

None listed

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