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NCT06095908

The Effect of Bilateral Rectus Sheath Block Versus Wound Infiltration in Gynecooncological Patients

Completed Last updated 24 May 2024
What this trial tests

trial testing Bupivacain in Postoperative Pain in 30 participants. Completed in 25 November 2023.

Timeline
15 June 2023
Primary endpoint
25 November 2023
25 November 2023

Quick facts

Lead sponsorDr. Lutfi Kirdar Kartal Training and Research Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date15 June 2023
Primary completion25 November 2023
Estimated completion25 November 2023
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Dr. Lutfi Kirdar Kartal Training and Research Hospital

Who can join

Adults 18 to 65, female only, with Postoperative Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Postoperative pain is a serious problem in gynecological oncology patients who underwent median vertical incision. The aim of our study is to compare ultrasound guided bilateral rectus sheath block and local anesthetic wound infiltration application in postoperative pain control.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Bupivacain

Trials testing the same drug.

Other recruiting trials for Postoperative Pain

Currently open trials in the same condition.

Other Dr. Lutfi Kirdar Kartal Training and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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