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NCT06120088

U.S. Guided Erector Spinae Block for Postoperative Pain Management in Paraumbilical Hernia Repair Patients

Status unknown Last updated 7 November 2023
What this trial tests

trial testing Bubpivacaine in Regional Anesthesia in 300 participants. Status unknown.

Timeline
1 December 2023
Primary endpoint
1 December 2024
1 January 2025

Quick facts

Lead sponsorAssiut University
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment300
Start date1 December 2023
Primary completion1 December 2024
Estimated completion1 January 2025

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 60, any sex, with Regional Anesthesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Abdominal surgery is one of the most definitive and mainstay treatment options for abdominal pathologies in clinical practice. Acute postoperative pain is a major challenge in the postoperative period. Although opioids are commonly used for analgesia after paraumbilical hernia, they can lead to side effects, such as nausea and vomiting, constipation, pruritus, and life-threatening respiratory depression. Regional anesthetic techniques are commonly used to prevent or minimize these side effects. The objective of this study is to assess the effectiveness of erector spinae plane block (ESPB) and standard medical (no block) pain management after paraumbilical hernia.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Bubpivacaine

Trials testing the same drug.

Other recruiting trials for Regional Anesthesia

Currently open trials in the same condition.

Other Assiut University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06120088.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing