clinical trial to study analgesic efficacy of external oblique fascial plane block in postoperative patients

Analgesic efficacy of external oblique plane block in multimodal regimen for postoperative pain after upper abdomen surgery: A prospective randomised, double-blind study

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/04/051315

Enrollment

Registered

2023-04-05

Start date

Unknown

Completion date

Unknown

Last updated

2024-08-19

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: External oblique fascial plane block.: Patient will be given General anaesthesia with external oblique fascial plane block with the single injection of ropivacaine 0.375% (20 ml) before

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex in the age group of 18 to 70 years with physical status ASA1 or ASA II

Exclusion criteria

Exclusion criteria: Consent refusal, Allergic history to local anaesthetic, abnormal coagulation profile, emergency surgeries, contraindications to regional anaesthesia

Design outcomes

Primary

Measure	Time frame
To evaluate the time to first analgesic request postoperatively.Timepoint: 1 year	—

Secondary

Measure	Time frame
1) NRS Scores, PONV scores, Pruritus, Sedation, respiratory depression, total dose of fentanyl used in 24 hour postoperatively 2) complications related to blockTimepoint: 1 year	—

Countries

India

Contacts

Public Contactgopal krishan jalwal

AIIMS, Bathinda

gopaljalwal@gmail.com07838939833

Outcome results

None listed

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