# Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section

> **NCT02714179** · PHASE4 · COMPLETED · sponsor: **Baskent University** · enrollment: 54 (actual)

## Conditions studied

- Cesarean Section; Dehiscence

## Interventions

- **DRUG:** Paracetamol was given intravenously in both group at different times

## Key facts

- **NCT ID:** NCT02714179
- **Lead sponsor:** Baskent University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2015-05
- **Primary completion:** 2016-01
- **Final completion:** 2016-01
- **Target enrollment:** 54 (ACTUAL)
- **Last updated:** 2016-03-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT02714179

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT02714179, "Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section". Retrieved via AI Analytics 2026-06-04 from https://api.ai-analytics.org/clinical/NCT02714179. Licensed CC0.

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