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NCT05365607 · ClinicalTrials.gov registry record · NA
NightWare and Cardiovascular Health in Adults With PTSD
A NA study of Cardiovascular Diseases and Posttraumatic Stress Disorder, sponsored by University of Colorado, Denver.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
- 2
- Study locations
NCT05365607 is a NA study of Cardiovascular Diseases and Posttraumatic Stress Disorder that has completed, run by University of Colorado, Denver. The registered enrollment target is 40 participants, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT05365607, a NA study of Cardiovascular Diseases and Posttraumatic Stress Disorder, has completed, sponsored by University of Colorado, Denver.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to determine whether NightWare therapeutic intervention improves biomarkers of vascular aging and autonomic function in adults with nightmares related to PTSD.
Conditions Studied
Interventions
- DEVICE NightWare
- DEVICE Sham NightWare
Study Locations (2)
Colorado
- University of Colorado Anschutz Medical Campus - Aurora
- University of Colorado CCTSI CTRC - Denver
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2022-06-24 |
| Est. Completion | 2024-08-18 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05365607
The ClinicalTrials.gov registry entry for NCT05365607 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The listed sponsor is University of Colorado, Denver, which has 1,283 total studies on file at ClinicalTrials.gov.
The record links to 6 conditions, with Cardiovascular Diseases appearing as the primary indexed condition, and to 2 interventions - of which NightWare is the first listed.
NCT05365607 reports 2 study locations spanning 1 distinct geographic area - top geographies include Colorado.
Frequently Asked Questions
What is clinical trial NCT05365607 about?
NCT05365607 is a clinical study titled "NightWare and Cardiovascular Health in Adults With PTSD". The purpose of this study is to determine whether NightWare therapeutic intervention improves biomarkers of vascular aging and autonomic function in adults with nightmares related to PTSD.
What is the current status of trial NCT05365607?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2022-06-24. Estimated completion is 2024-08-18.
What conditions does trial NCT05365607 study?
This clinical trial studies the following conditions: Cardiovascular Diseases, Posttraumatic Stress Disorder, Endothelial Dysfunction, Vascular Stiffness, Autonomic Dysfunction.
What interventions are being tested in trial NCT05365607?
The interventions under investigation include: NightWare (DEVICE), Sham NightWare (DEVICE).
Who is sponsoring clinical trial NCT05365607?
This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05365607 being conducted?
This trial has 2 study locations across Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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