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Oxidative Stress and Cardiovascular Morbidity in Sleep Apnea-Hypopnea Syndrome (SAHS) (OSCAMSA)

Primary Purpose

Sleep Apnea, Cardiovascular Diseases

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
nasal CPAP
Sham CPAP
Sponsored by
Hospital Universitario La Paz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Sleep Apnea focused on measuring sleep apnea, morbidity, cardiovascular, cpap, oxidative stress

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Sleep apnea-hypopnea syndrome (AHI > 5)
  • Excessive sleepiness (ESS > 11)
  • No previous CPAP treatment

Exclusion Criteria:

  • Blood pressure > 180/120 mmHg.
  • Secondary hypertension
  • Professional driver
  • COPD, asthma, bronchiectasis, lung cancer, restrictive lung disorder, chest wall disease
  • Neuromuscular disease or thyroid function abnormalities
  • Morbid obesity (BMI > 40 Kg/m2).
  • Respiratory infection in the 2 last months.
  • Anemia (Hb < 10 g/dl) or polyglobulia (Hct > 55%).
  • Diurnal hypercapnia (PaCO2 > 45 mmHg) or moderate hypoxemia (PaO2 < 70 mmHg).

Sites / Locations

  • Hospital Universitario La Paz

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

CPAP

Sham CPAP

Arm Description

Continuous positive airway pressure

Sham nasal continuous positive airway pressure

Outcomes

Primary Outcome Measures

Plasmatic 8-isoprostane concentration

Secondary Outcome Measures

Plasmatic and condensed exhaled air concentrations of homocysteine, HIF-1, NFkB, AP-1, VEGF, ET-1, TNF-alpha, IL-1, IL-6, ICAM-1, VCAM-1, nitrates and nitrites.

Full Information

First Posted
June 18, 2007
Last Updated
April 1, 2013
Sponsor
Hospital Universitario La Paz
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1. Study Identification

Unique Protocol Identification Number
NCT00487929
Brief Title
Oxidative Stress and Cardiovascular Morbidity in Sleep Apnea-Hypopnea Syndrome (SAHS)
Acronym
OSCAMSA
Official Title
Phase 4 Study of the Relationship Between the Oxidative Stress and the Development of Cardiovascular Complications in the Sleep Apnea-hypopnea Syndrome (SAHS). Effect of the Treatment With CPAP
Study Type
Interventional

2. Study Status

Record Verification Date
October 2008
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Hospital Universitario La Paz

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to compare the levels of 8-isoprostane and other oxidative stress biomarkers in plasma and condensed exhaled air between patients with SAHS and cardiovascular complications, patients with SAHS without cardiovascular complications and control subjects. To evaluate the effect of three months of treatment with CPAP on the oxidative stress biomarkers.
Detailed Description
Aim: To compare the levels of 8-isoprostane and other oxidative stress biomarkers in plasma and condensed exhaled air between patients with SAHS and cardiovascular complications, patients with SAHS without cardiovascular complications and control subjects. To evaluate the effect of three months of treatment with CPAP on the oxidative stress biomarkers. Design: randomized, double blind, of parallel groups and controlled with placebo study. Study subjects: 53 patients with SAHS (23 with cardiovascular complications and 30 without cardiovascular complications), 23 patients with cardiovascular diseases without SAHS and 23 control subjects. Interventions: Three months of treatment with therapeutic CPAP or with sham CPAP (placebo). Determinations: clinical (cardiovascular morbidity) and anthropometric data. Fat free corporal mass, echocardiography, spirometry, ambulatory monitoring of the arterial pressure, endothelial reactivity. Oxidative stress biomarkers (8-isoprostane, homocysteine, HIF-1, NFkB, AP-1, VEGF, ET-1, TNF-alpha, IL-1, IL-6, ICAM-1, VCAM-1, nitrates and nitrites) in plasma and condensed exhaled air.Peripheral sensitivity to hypoxia. Urinary excretion of catecholamines.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sleep Apnea, Cardiovascular Diseases
Keywords
sleep apnea, morbidity, cardiovascular, cpap, oxidative stress

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CPAP
Arm Type
Experimental
Arm Description
Continuous positive airway pressure
Arm Title
Sham CPAP
Arm Type
Sham Comparator
Arm Description
Sham nasal continuous positive airway pressure
Intervention Type
Device
Intervention Name(s)
nasal CPAP
Intervention Description
Nocturnal
Intervention Type
Device
Intervention Name(s)
Sham CPAP
Intervention Description
Nocturnal
Primary Outcome Measure Information:
Title
Plasmatic 8-isoprostane concentration
Time Frame
three months
Secondary Outcome Measure Information:
Title
Plasmatic and condensed exhaled air concentrations of homocysteine, HIF-1, NFkB, AP-1, VEGF, ET-1, TNF-alpha, IL-1, IL-6, ICAM-1, VCAM-1, nitrates and nitrites.
Time Frame
three months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Sleep apnea-hypopnea syndrome (AHI > 5) Excessive sleepiness (ESS > 11) No previous CPAP treatment Exclusion Criteria: Blood pressure > 180/120 mmHg. Secondary hypertension Professional driver COPD, asthma, bronchiectasis, lung cancer, restrictive lung disorder, chest wall disease Neuromuscular disease or thyroid function abnormalities Morbid obesity (BMI > 40 Kg/m2). Respiratory infection in the 2 last months. Anemia (Hb < 10 g/dl) or polyglobulia (Hct > 55%). Diurnal hypercapnia (PaCO2 > 45 mmHg) or moderate hypoxemia (PaO2 < 70 mmHg).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco García-Rio, PhD
Organizational Affiliation
Servicio de Neumología. Hospital Universitario La Paz
Official's Role
Study Chair
Facility Information:
Facility Name
Hospital Universitario La Paz
City
Madrid
ZIP/Postal Code
28046
Country
Spain

12. IPD Sharing Statement

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Oxidative Stress and Cardiovascular Morbidity in Sleep Apnea-Hypopnea Syndrome (SAHS)

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