# Responsiveness Index Versus the RASS Based Method for Adjusting Sedation in Critically Ill Patients

> **NCT03250481** · NA · COMPLETED · sponsor: **Helsinki University Central Hospital** · enrollment: 32 (actual)

## Conditions studied

- Critical Illness

## Interventions

- **DRUG:** Propofol

## Key facts

- **NCT ID:** NCT03250481
- **Lead sponsor:** Helsinki University Central Hospital
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2013-03
- **Primary completion:** 2017-08-28
- **Final completion:** 2017-08-28
- **Target enrollment:** 32 (ACTUAL)
- **Last updated:** 2019-08-15


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT03250481

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT03250481, "Responsiveness Index Versus the RASS Based Method for Adjusting Sedation in Critically Ill Patients". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT03250481. Licensed CC0.

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