# Towards Enhanced Recovery After Cesarean

> **NCT04612920** · EARLY_PHASE1 · COMPLETED · sponsor: **University of Oklahoma** · enrollment: 33 (actual)

## Conditions studied

- Cesarean Section Complications

## Interventions

- **DRUG:** Ibuprofen, acetaminophen, oxycodone

## Key facts

- **NCT ID:** NCT04612920
- **Lead sponsor:** University of Oklahoma
- **Sponsor class:** OTHER
- **Phase:** EARLY_PHASE1
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2020-12-12
- **Primary completion:** 2023-03-08
- **Final completion:** 2023-03-08
- **Target enrollment:** 33 (ACTUAL)
- **Last updated:** 2023-03-14


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04612920

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04612920, "Towards Enhanced Recovery After Cesarean". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT04612920. Licensed CC0.

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