# Evaluation of the Typical Spinal Block During Cesarean Delivery

> **NCT06206044** · — · ENROLLING_BY_INVITATION · sponsor: **Oregon Health and Science University** · enrollment: 250 (estimated)

## Conditions studied

- Cesarean Section
- Anesthesia, Obstetric

## Interventions

- **DRUG:** Intrathecal 1.6 ml 0.75% bupivacaine in 8.25% dextrose combined with 15 mcg fentanyl and 150 mcg preservative-free morphine

## Key facts

- **NCT ID:** NCT06206044
- **Lead sponsor:** Oregon Health and Science University
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** ENROLLING_BY_INVITATION
- **Start date:** 2024-06-10
- **Primary completion:** 2025-12-31
- **Final completion:** 2026-01-31
- **Target enrollment:** 250 (ESTIMATED)
- **Last updated:** 2024-11-20


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT06206044

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT06206044, "Evaluation of the Typical Spinal Block During Cesarean Delivery". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT06206044. Licensed CC0.

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