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Trial · NCT01637584

Neurobiology of Sleep and Sleep Treatment Response in Returning Veterans

NCT01637584, Not applicable, Completed, University of Pittsburgh; results first posted 2017-04-17

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Neurobiology of Sleep and Sleep Treatment Response in Returning Veterans. Trials, record NCT01637584. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01637584

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Neurobiology of Sleep and Sleep Treatment Response in Returning Veterans
NCT number
NCT01637584
Status
Completed
Phases
Not applicable
Enrollment
40 participants, actual
Lead sponsor
University of Pittsburgh
Conditions
Non PTSD, PTSD
Interventions
Prazosin, Placebo
First posted
2012-07-11
Last updated
2017-05-23
Results first posted
2017-04-17

Source ClinicalTrials.gov

Registered outcomes2

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryWhole Brain Relative Regional Cerebral Metabolic Rate of GlucoseBaseline and post-intervention at 8-10 weeks
The reported Z value reflect the magnitude of the state difference (Wake vs. Non-REM or Wake vs. REM) within the prazosin group pre-to-post treatment, and after using a mask to adjust for the spurious effects of the passage of time.
SecondaryPittsburgh Sleep Quality Index (PSQI):Baseline and post-treatment at 8-10 weeksSelf-report sleep quality measure. Scores range from 0 to 21, with higher scores reflecting poorer sleep quality.

Outcomes2

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYWhole Brain Relative Regional Cerebral Metabolic Rate of GlucoseBaseline and post-intervention at 8-10 weeks
9 of the 20 participants who were randomized to prazosin and 13 of the participants randomized to placebo provided scans pre- and post-treatment that were of sufficiency quality to be included in the final analyses.
Z valuesNUMBER
SECONDARYPittsburgh Sleep Quality Index (PSQI):Baseline and post-treatment at 8-10 weeks
9 of the 20 participants who were randomized to prazosin and 13 of the participants randomized to prazosin provided scans pre- and post-treatment that were of sufficiency quality to be included in the final analyses.
units on a scaleMEAN

Results by group10

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboPre-to-Post Treatment (Wakefulness > NREM)3.78Z values
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboPre-to-Post Treatment (Wakefulness < NREM)3.76Z values
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboPre-to-Post Treatment (Wakefulness > REM)3.52Z values
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboPre-to-Post Treatment (Wakefulness < REM)3.36Z values
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboWithin-state time-dependent decrease in rCMRglc4.12Z values
Whole Brain Relative Regional Cerebral Metabolic Rate of GlucosePrazosin -PlaceboWithin-state time-dependent increase in rCMRglc3.89Z values
Pittsburgh Sleep Quality Index (PSQI):PrazosinPSQI: Baseline9.25Standard Deviation 2.64units on a scale
Pittsburgh Sleep Quality Index (PSQI):PlaceboPSQI: Baseline8.08Standard Deviation 2.72units on a scale
Pittsburgh Sleep Quality Index (PSQI):PrazosinPSQI: Post6.71Standard Deviation 4.31units on a scale
Pittsburgh Sleep Quality Index (PSQI):PlaceboPSQI: Post6.54Standard Deviation 2.57units on a scale

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPrazosin20
Overall StudySTARTEDPlacebo20
Overall StudyCOMPLETEDPrazosin19
Overall StudyCOMPLETEDPlacebo17
Overall StudyNOT COMPLETEDPrazosin1
Overall StudyNOT COMPLETEDPlacebo3

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 totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPrazosin
Total, all-cause mortalityPlacebo
Total, other adverse eventsPrazosin020
Total, other adverse eventsPlacebo020
Total, serious adverse eventsPrazosin020
Total, serious adverse eventsPlacebo020

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
24893322DERIVED

Source PubMed

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
Prazosin vs Placebo: serious adverse events

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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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/NCT01637584

GET https://conductscience.org/api/trials/v1/NCT01637584/registered