# Quality of Recovery After Dexamethasone, Ondansetron or Placebo Intrathecal Morphine Administration

> **NCT03035942** · PHASE4 · COMPLETED · sponsor: **Pontificia Universidade Catolica de Sao Paulo** · enrollment: 135 (actual)

## Conditions studied

- Fractures, Bone
- Nausea and Vomiting, Postoperative
- Pruritus
- Morphine Adverse Reaction
- Satisfaction, Personal

## Interventions

- **DRUG:** Dexamethasone
- **DRUG:** Ondansetron
- **DRUG:** Saline

## Key facts

- **NCT ID:** NCT03035942
- **Lead sponsor:** Pontificia Universidade Catolica de Sao Paulo
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2017-01-02
- **Primary completion:** 2018-10-01
- **Final completion:** 2019-11-04
- **Target enrollment:** 135 (ACTUAL)
- **Last updated:** 2020-03-19


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03035942

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03035942, "Quality of Recovery After Dexamethasone, Ondansetron or Placebo Intrathecal Morphine Administration". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT03035942. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*