Unknown PHASE4 INTERVENTIONAL 2-arm NCT04697277

Antibiotic Prophylaxis and Nausea and Vomiting in Cesarean Section Under Regional Anesthesia.

The Effect of Antibiotic Prophylaxis Timing on Intraoperative Nausea and Vomiting in Patients Undergoing Cesarean Section Under Regional Anesthesia.

Sponsor: Baskent University Ankara Hospital

Conditions Intraoperative Nausea-retching-vomiting Episodes Nausea Scores Will be Evaluated on the Verbal Analog Scale (VAS)

Interventions Antibiotic prophylaxis timing (before skin incision and after cord clamping) for caesarean section

Updated 5 times since 2021 Last updated: Jan 5, 2021 Started: Aug 20, 2015 Primary completion: Apr 30, 2021 Completion: May 30, 2021

This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE4 trial investigates Intraoperative Nausea-retching-vomiting Episodes and Nausea Scores Will be Evaluated on the Verbal Analog Scale (VAS) and is currently ongoing. Baskent University Ankara Hospital leads this study, which shows 5 recorded versions since 2015 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

Change History

5 versions recorded

Sep 2025 — Present [monthly]

Unknown PHASE4
Sep 2024 — Sep 2025 [monthly]

Unknown PHASE4
Jul 2024 — Sep 2024 [monthly]

Unknown PHASE4

Status: Unknown Status → Unknown
Feb 2023 — Jul 2024 [monthly]

Unknown Status PHASE4

Status: Recruiting → Unknown Status
Feb 2021 — Feb 2023 [monthly]

Recruiting PHASE4

First recorded

Aug 2015

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Baskent University Ankara Hospital

Data source: Baskent University Ankara Hospital

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Ankara, Turkey (Türkiye)