Trial · NCT04817410
Results by group51
Each measurement the trial posted, group by group, in the words and numbers it posted.
1 to 20 of 51
Download this page as JSON| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants Enrolled and Receiving Formal Addiction Treatment at Day 14 | Oral Naltrexone | Engaged in treatment at 14-days | 6 | Participants | |
| Number of Participants Enrolled and Receiving Formal Addiction Treatment at Day 14 | Oral Naltrexone | Not engaged in treatment at 14-days | 15 | Participants | |
| Number of Participants Enrolled and Receiving Formal Addiction Treatment at Day 30 | Enrolled Participant Characteristics | Engaged in treatment at 30-days | 7 | Participants | |
| Number of Participants Enrolled and Receiving Formal Addiction Treatment at Day 30 | Enrolled Participant Characteristics | Not engaged in treatment at 30-days | 14 | Participants | |
| Number of Alcoholic Drinks Per Day | Oral Naltrexone | 4.29 | Inter-Quartile Range 2.29 to 7.57 | # of drinks consumed per day | |
| Number of Daily Drinks | Enrolled Participant Characteristics | 0.73 | Inter-Quartile Range 0 to 2.81 | # of drinks consumed per day | |
| Daily Alcohol Craving Scale | Enrolled Participant Characteristics | 8.27 | Inter-Quartile Range 4.65 to 11.75 | score on a scale | |
| Guidelines Regimen Information Program (GRIP) Guide at Day 14 | Oral Naltrexone | 4.5 | Inter-Quartile Range 3 to 5 | units on a scale | |
| Guidelines Regimen Information Program (GRIP) Guide at Day 30 | Oral Naltrexone | 4 | Inter-Quartile Range 4 to 5 | units on a scale | |
| Number of Heavy Drinking Days | Oral Naltrexone | 0.0 | Inter-Quartile Range 0 to 0.17 | days | |
| Health Services Utilization Survey | Oral Naltrexone | Inpatient Admissions - baseline | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | outpatient visits -baseline | 0 | Inter-Quartile Range 0 to 1 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | ED visits - baseline | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | Inpatient admissions-day 14 preceding 7-days at baseline) | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | Outpatient visits-day 14 | 0.5 | Inter-Quartile Range 0 to 1 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | Emergency Department Visits - day 14 | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | Inpatient admission - day 30 | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | Outpatient visits - day 30 | 0 | Inter-Quartile Range 0 to 1 | number of occurrences |
| Health Services Utilization Survey | Oral Naltrexone | ED visits - day 30 | 0 | Inter-Quartile Range 0 to 0 | number of occurrences |
| Number of Unhealthy Days Assessed by Health Related Quality of Life (HRQoL) | Oral Naltrexone | 11.5 | Inter-Quartile Range 0 to 30 | unhealthy days |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
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.
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GET https://conductscience.org/api/trials/v1/NCT04817410/results