# Sedative Premedication: Efficacy On Patient Experience

> **NCT01901003** · PHASE3 · COMPLETED · sponsor: **Assistance Publique Hopitaux De Marseille** · enrollment: 1200 (actual)

## Conditions studied

- Perioperative Anxiety

## Interventions

- **DRUG:** Lorazepam
- **OTHER:** no premedication
- **DRUG:** Placebo (microcrystalline celluloses)

## Key facts

- **NCT ID:** NCT01901003
- **Lead sponsor:** Assistance Publique Hopitaux De Marseille
- **Sponsor class:** OTHER
- **Phase:** PHASE3
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2012-11
- **Primary completion:** 2014-06
- **Final completion:** 2014-06
- **Target enrollment:** 1200 (ACTUAL)
- **Last updated:** 2015-04-21


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01901003

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01901003, "Sedative Premedication: Efficacy On Patient Experience". Retrieved via AI Analytics 2026-05-28 from https://api.ai-analytics.org/clinical/NCT01901003. Licensed CC0.

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