# Effect of Propofol Administration Time on the Incidence and Severity of Intrathecal Morphine-induced Pruritus in Parturient Undergoing Elective Cesarean Delivaries

> **NCT06715657** · PHASE4 · NOT_YET_RECRUITING · sponsor: **Assiut University** · enrollment: 204 (estimated)

## Conditions studied

- Cesarean Section

## Interventions

- **DRUG:** Morphine intrathecal
- **DRUG:** propofol
- **DRUG:** propofol

## Key facts

- **NCT ID:** NCT06715657
- **Lead sponsor:** Assiut University
- **Sponsor class:** OTHER
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** NOT_YET_RECRUITING
- **Start date:** 2024-12-01
- **Primary completion:** 2026-12-01
- **Final completion:** 2027-01-01
- **Target enrollment:** 204 (ESTIMATED)
- **Last updated:** 2024-12-04


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06715657

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06715657, "Effect of Propofol Administration Time on the Incidence and Severity of Intrathecal Morphine-induced Pruritus in Parturient Undergoing Elective Cesarean Delivaries". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT06715657. Licensed CC0.

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