Trial · NCT03021486
Outcomes11
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Change in Richmond Agitation Sedation Score (RASS) (0-24h) | Time 0 or Baseline and 24 hours after study medication administration | Analysis included 31 participants who completed 24 hours of the study. | score on a scale | MEAN |
| SECONDARY | Percentage of Participants With RASS Score -2 to 0 | Time 0 or Baseline and 24 hours later. | Analysis included 31 participants who completed 24 hours of the study. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Change in RASS Score (0-30 Minutes) | Time 0 or Baseline and 30 minutes later. | Analysis included 45 participants who completed first 30 minutes of study | score on a scale | MEAN |
| SECONDARY | Number of Participants With RASS Score of >=1 | 0 or Baseline and 24 hours later | Analysis included 45 participants who completed first 24 hours of study | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Pattern of Medication Use | Baseline and 24 hours | Analysis included 45 participants who were still on study. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Perceived Comfort Level as Assessed by Caregiver | Baseline and 24 hour | Analysis included 37 participants who completed this questionnaire at that time point | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Perceived Comfort Level as Assessed by Nurse | Baseline and 24 hour | Analysis included 37 participants who completed this questionnaire at that time point | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Change in Delirium Experience Questionnaire | Baseline and Day 3 | Analysis included 37 participants who completed this questionnaire at that time point. | score on a scale | MEAN |
| SECONDARY | Memorial Delirium Assessment Scale (MDAS) | Baseline and 24 hours | Analysis included 30 participants who completed this questionnaire at that time point | score on a scale | MEAN |
| SECONDARY | Edmonton Expression Assessment System, ESAS | Baseline and 24 hours | Analysis included 33 participants who completed this questionnaire at that time point. Note that 9 participants completed 'feeling of well being' question for Combination group, and 13 participants completed 'pain' and 'sleep' questions for Escalation group | score on a scale | MEAN |
| SECONDARY | Udvalg for Kliniske Undersogelser, UKU | Baseline and 3 days | Analysis included 25 participants who were still on study | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT03021486/outcomes