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Impact of Continuous Positive Airway Pressure Therapy on Bilateral Local Hippocampal Gray Matter Volume in Elderly Patients With Obstructive Sleep Apnea - Study BBBSAS

NCT07882433, Not applicable, Not yet recruiting, Centre Hospitalier Universitaire de Saint Etienne

Trial 10

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

FieldValueSource
TitleImpact of Continuous Positive Airway Pressure Therapy on Bilateral Local Hippocampal Gray Matter Volume in Elderly Patients With Obstructive Sleep Apnea - Study BBBSASClinicalTrials.gov
NCT numberNCT07882433ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment50 participants, estimatedClinicalTrials.gov
Lead sponsorCentre Hospitalier Universitaire de Saint EtienneClinicalTrials.gov
ConditionsHypopnea Syndrome, Apnea, Obstructive SleepClinicalTrials.gov
InterventionsContinuous Positive Airway Pressure (CPAP) therapy, Multimodal brain MRI with Gadolinium injectionClinicalTrials.gov
First posted2026-10-20ClinicalTrials.gov
Last updated2026-10-20ClinicalTrials.gov

Registered outcomes 6

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

ListOutcomeTime frameDescriptionSource
PrimaryBlood-brain barrier (BBB) permeability abnormality in the hippocampus and frontal cortexmonths 6
Assessed using a multimodal MRI protocol (3D T1 MP2RAGE, T2 relaxometry, diffusion tensor imaging, T2\* susceptibility-weighted imaging, dynamic contrast-enhanced perfusion imaging providing the permeability-surface area product \[PS\], and post-Gadolinium 3D T1 MPRAGE), analyzed by voxel-based morphometry and automated hippocampal segmentation.
ClinicalTrials.gov
SecondaryBlood-brain barrier (BBB) permeability abnormality in the hippocampus and frontal cortexmonths : 6
Assessed using a multimodal MRI protocol (3D T1 MP2RAGE, T2 relaxometry, diffusion tensor imaging, T2\* susceptibility-weighted imaging, dynamic contrast-enhanced perfusion imaging providing the permeability-surface area product \[PS\], and post-Gadolinium 3D T1 MPRAGE), analyzed by voxel-based morphometry and automated hippocampal segmentation.
ClinicalTrials.gov
SecondaryLocal white matter volume6 monthsVoxel-level gray-scale analysis of white matter, using the same MRI acquisitions and analysis pipeline as the primary outcome.ClinicalTrials.gov
SecondaryDysexecutive / memory cognitive score6 monthsComposite score derived from a neuropsychological battery (Stroop test, Trail Making Test A/B, verbal fluency, digit span, WAIS-III subtests, free/cued recall, PASAT).ClinicalTrials.gov
SecondaryDual-task gait and balance performance6 monthsStep variability and balance time under single- and dual-task walking conditions, measured with pressure-sensor insoles and a force platform.ClinicalTrials.gov
SecondarySystemic inflammatory and aquaporin biomarkers6 monthsSerum hs-CRP, IL-1β, IL-6, IL-10, TNF-α and MCP-1 (Luminex®); serum and urinary aquaporin 1 and 3 (ELISA).ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

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

ComparisonSource

Tests 6

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Digit Span TestSecondary outcomeConductCognition
Paced Visual Serial Addition TestSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition
Verbal FluencySecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)