NCT00456287

Brief Summary

The objective of the study is to define and compare clotting- fibrinolysis patterns, platelet function markers and endothelial dysfunction in patients with SAHS before and after treatment and normal controls age and weight matched.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2007

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

April 2, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

April 4, 2007

Completed
Last Updated

April 4, 2007

Status Verified

April 1, 2007

First QC Date

April 2, 2007

Last Update Submit

April 2, 2007

Conditions

Sleep ApneaCardiovascular Diseases

Keywords

Sleep ApneaClotting- fibrinolysis patternsPlatelet function markersEndothelial dysfunction

Outcome Measures

Primary Outcomes (1)

  • To define and compare clotting- fibrinolysis patterns, platelet function markers and endothelial dysfunction

Secondary Outcomes (1)

  • CPAP (Continuous Positive Airway Pressure) effect on studied variables

Interventions

CPAP (Continuous Positive Airway Pressure)DEVICE

Eligibility Criteria

Age25 Years - 65 Years
Sexmale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Apnea-Hypopnea Index \> 15

You may not qualify if:

  • Presence of any chronic disease
  • Presence of cardiovascular disease
  • Refusal to sign informed consent
  • Drug addiction and/or alcoholism
  • Any medication two weeks before

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hospital Universitario Son Dureta

Palma de Mallorca, Balearic Islands, 07014, Spain

RECRUITING

MeSH Terms

Conditions

Sleep Apnea SyndromesCardiovascular Diseases

Interventions

Continuous Positive Airway Pressure

Condition Hierarchy (Ancestors)

ApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System Diseases

Intervention Hierarchy (Ancestors)

Positive-Pressure RespirationRespiration, ArtificialAirway ManagementTherapeuticsRespiratory Therapy

Study Officials

  • Antonia Barceló, MD

    Hospital Universitario Son Dureta

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Antonia Barceló, MD

CONTACT

34 971 175112abarcelo@hsd.es

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

April 2, 2007

First Posted

April 4, 2007

Study Start

February 1, 2007

Last Updated

April 4, 2007

Record last verified: 2007-04

Locations

ES(1)