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NCT06138938

Effects of Abdominal Irrigation During Cesarean

Completed NA Last updated 18 November 2023
What this trial tests

NA trial testing Intraoperative abdominal irrigation in Cesarean Section in 60 participants. Completed in 30 June 2022.

Timeline
1 March 2022
Primary endpoint
31 May 2022
30 June 2022

Quick facts

Lead sponsorIstanbul Medeniyet University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposeother
Enrollment60
Start date1 March 2022
Primary completion31 May 2022
Estimated completion30 June 2022
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Istanbul Medeniyet University

Who can join

Adults 18 to 45, female only, with Cesarean Section or Visual Analog Scale. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This prospective randomized controlled clinical trial was conducted between March 2022 and May 2022 and included 60 patients who underwent elective cesarean. The participants were randomized into two groups: abdominal irrigation (n=30) and control group (n=30). Participants undergo a standard cesarean procedure, and general anesthesia was preferred. The patients were questioned regarding nausea, vomiting, highest pain scores, time of flatus, and stool passage during the postoperative period.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Erratum.
    · 2023 · PMID 38148729 · DOI 10.4274/mmj.galenos.2023.e002

Verify or expand the search:

Other recruiting trials for Cesarean Section

Currently open trials in the same condition.

Other Istanbul Medeniyet 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/NCT06138938.

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