Trial · NCT07596342
Electrophysiological Analysis of Gamma-Hydroxybutyrate-induced Sleep in Intensive Care Patients
NCT07596342, Phase 2, Not yet recruiting, Assistance Publique - Hôpitaux de Paris
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Electrophysiological Analysis of Gamma-Hydroxybutyrate-induced Sleep in Intensive Care Patients. Trials, record NCT07596342. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07596342
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Electrophysiological Analysis of Gamma-Hydroxybutyrate-induced Sleep in Intensive Care Patients
- NCT number
- NCT07596342
- Status
- Not yet recruiting
- Phases
- Phase 2
- Enrollment
- 24 participants, estimated
- Lead sponsor
- Assistance Publique - Hôpitaux de Paris
- Conditions
- Sleep Disorder (Disorder), Critical Care
- Interventions
- GHB, Placebo
- First posted
- 2026-05-19
- Last updated
- 2026-05-22
Source ClinicalTrials.gov
Registered outcomes24
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Deep slow-wave sleep | During the night between the day of enrollment (Day0) and the next day (Day 1). | The primary endpoint is the duration (in minutes) of deep slow-wave sleep (N3 stage) based on polysomnographic recordings. |
| Secondary | Sleep onset latency | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Total sleep time | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Duration of N1 stage | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Percentage of N1 stage | During the night between the day of enrollment (Day0) and the next day (Day 1) | |
| Secondary | Duration of N2 stage | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Percentage of N2 stage | During the night between the day of enrollment (Day0) and the next day (Day 1) | |
| Secondary | Percentage of N3 stage | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Duration of Rapid Eye Movement sleep | During the night between the day of enrollment (Day0) and the next day (Day 1). | |
| Secondary | Percentage of Rapid Eye Movement sleep | During the night between the day of enrollment (Day0) and the next day (Day 1) |
1 to 10 of 24Source ClinicalTrials.gov
See all 24 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07596342
GET https://conductscience.org/api/trials/v1/NCT07596342/registered?page=2