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Effect of CPAP Treatment in Women With Moderate-to-severe OSA.

Primary Purpose

Obstructive Sleep Apnea

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Continuous positive airways pressure
Sponsored by
Francisco Campos-Rodriguez
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Obstructive Sleep Apnea focused on measuring Obstructive sleep apnea, Female gender, Continuous Positive Airway Pressure

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Moderate-to-severe OSA (Apnea-Hypopnea index ≥15) diagnosed by Home Respiratory Polygraphy.
  • Age between 18-75 years.

Exclusion Criteria:

  • diagnosis of narcolepsy or restless legs syndrome
  • unstable cardiovascular profile (cardiovascular event in the previous 3 months)
  • cancer or life expectancy lower than 1 year
  • uncontrolled psychiatric disorders
  • central sleep apnea (>50% of central events)
  • pregnancy
  • risky jobs and severe hypersomnolence (Epworth >=18) requiring urgent treatment
  • either respiratory failure (SaO2<90% or partial oxygen pressure [pO2] <60 mmHg or Long-term O2 therapy
  • heart failure (New York Heart Association class III-IV)
  • prior CPAP therapy

Sites / Locations

  • Hospital Universitario Valme

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard Care

Continuous positive airways pressure

Arm Description

Conservative treatment. This group will be receive standard care for OSA consisting of hygienic-dietary advice and lifestyle counseling.

Optimal Continuous positive airways pressure treatment every night plus standard care for OSA consisting of hygienic-dietary advice and lifestyle counseling.

Outcomes

Primary Outcome Measures

Change from baseline in quality of life on the Quebec Sleep Questionnaire (QSQ) at week 12

Secondary Outcome Measures

Change from baseline in quality of life on the 12-Item Short Form Health Survey (SF-12) at week 12
Change from baseline in mood state on the Abbreviated Profile Of Mood States (POMS) at week 12
Change from baseline in sleepiness on the Epworth Sleepiness Score (ESS) at week 12
Change from baseline in anxiety and depression on the Hospital Anxiety and Depression questionnaire (HAD) at week 12
Change from baseline in quality of life on the Visual Analogic Scale (VAS) at week 12
Change from baseline in sleep apnea symptoms at week 12
Change from baseline in blood pressure at week 12
Change in office blood pressure from baseline at week 12
Change from baseline in glucose metabolism at week 12
Change from baseline in lipid metabolism at week 12

Full Information

First Posted
January 19, 2014
Last Updated
August 17, 2015
Sponsor
Francisco Campos-Rodriguez
Collaborators
Fondo de Investigacion Sanitaria, Sociedad Española de Neumología y Cirugía Torácica
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1. Study Identification

Unique Protocol Identification Number
NCT02047071
Brief Title
Effect of CPAP Treatment in Women With Moderate-to-severe OSA.
Official Title
Effect of Continuous Positive Airways Pressure (CPAP) in Women With Moderate-to-severe Obstructive Sleep Apnea (OSA). A Multicenter, Randomized, Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
February 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Francisco Campos-Rodriguez
Collaborators
Fondo de Investigacion Sanitaria, Sociedad Española de Neumología y Cirugía Torácica

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether Continuous Positive Airways Pressure (CPAP) improves quality of life, cardiovascular (blood pressure) and metabolic profile (glucose and lipid metabolism) in females with moderate-to-severe Obstructive Sleep Apnea (OSA).
Detailed Description
Study Design: multicenter, open-label, randomized, controlled trial of parallel groups with a final blind evaluation. Study sites. The following hospitals will participate in the study: Valme (Sevilla), la Fe (Valencia), Virgen del Rocío (Sevilla), Gral Yagüe (Burgos), San Pedro de Alcántara (Cáceres), Dr Peset (Valencia), Severo Ochoa (Madrid), Reina Sofía (Córdoba), Dr Negrín (Las Palmas de Gran Canaria), Virgen de la Victoria (Málaga), Río Hortega (Valladolid), Costa del Sol (Málaga), Marqués de Valdecilla (Santander), Albacete (Albacete), Virgen del Puerto (Cáceres), Puerta de Hierro (Madrid), Consorcio Sanitario de Terrassa (Barcelona), Getafe (Madrid), Gral de Alicante (Alicante), Morales Meseguer (Murcia), Tomelloso (Ciudad Real), and Fundación Jiménez Díaz (Madrid). All centers from Spain. Methods: consecutive outpatient women aged 18-75 years and referred to the sleep clinics for suspicion of OSA will be studied. They will undergo a diagnostic home respiratory polygraphy, and those diagnosed with moderate-to-severe OSA (AHI ≥15) will be eligible for this study and randomized to optimal CPAP treatment or conservative treatment for 12 weeks. Every women will fulfill a standardized protocol and different quality of life questionnaires. Office blood pressure will be measured. Fasting blood samples will be collected to assess glucose and lipid metabolism. All the measurements will be performed at baseline and after 12 weeks of follow-up. Women will be examined at the time of inclusion, after 4 weeks of follow-up and at the end of follow-up (12 weeks). 149 women with moderate-to-severe OSA need to be enrolled in each study arm, according to the sample size calculated to achieve a clinically significant improvement in the Quebec Sleep Questionnaire. The results will be analyzed both on an intention-to-treat basis and on a per-protocol basis (data only from patients who finish the study and show good adherence to CPAP, defined as an average objective use of at least 4 hours/day).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obstructive Sleep Apnea
Keywords
Obstructive sleep apnea, Female gender, Continuous Positive Airway Pressure

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
307 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Care
Arm Type
No Intervention
Arm Description
Conservative treatment. This group will be receive standard care for OSA consisting of hygienic-dietary advice and lifestyle counseling.
Arm Title
Continuous positive airways pressure
Arm Type
Experimental
Arm Description
Optimal Continuous positive airways pressure treatment every night plus standard care for OSA consisting of hygienic-dietary advice and lifestyle counseling.
Intervention Type
Device
Intervention Name(s)
Continuous positive airways pressure
Intervention Description
Optimal Continuous positive airways pressure treatment every night plus standard care for OSA consisting of hygienic-dietary advice and lifestyle counseling.
Primary Outcome Measure Information:
Title
Change from baseline in quality of life on the Quebec Sleep Questionnaire (QSQ) at week 12
Time Frame
Baseline, 12 weeks.
Secondary Outcome Measure Information:
Title
Change from baseline in quality of life on the 12-Item Short Form Health Survey (SF-12) at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in mood state on the Abbreviated Profile Of Mood States (POMS) at week 12
Time Frame
Baseline, 12 weeks
Title
Change from baseline in sleepiness on the Epworth Sleepiness Score (ESS) at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in anxiety and depression on the Hospital Anxiety and Depression questionnaire (HAD) at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in quality of life on the Visual Analogic Scale (VAS) at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in sleep apnea symptoms at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in blood pressure at week 12
Description
Change in office blood pressure from baseline at week 12
Time Frame
Baseline, 12 weeks
Title
Change from baseline in glucose metabolism at week 12
Time Frame
baseline, 12 weeks
Title
Change from baseline in lipid metabolism at week 12
Time Frame
baseline, 12 weeks
Other Pre-specified Outcome Measures:
Title
Number of Participants with CPAP use >= 4 hours/day as a Measure of CPAP adherence
Time Frame
Baseline, 12 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Moderate-to-severe OSA (Apnea-Hypopnea index ≥15) diagnosed by Home Respiratory Polygraphy. Age between 18-75 years. Exclusion Criteria: diagnosis of narcolepsy or restless legs syndrome unstable cardiovascular profile (cardiovascular event in the previous 3 months) cancer or life expectancy lower than 1 year uncontrolled psychiatric disorders central sleep apnea (>50% of central events) pregnancy risky jobs and severe hypersomnolence (Epworth >=18) requiring urgent treatment either respiratory failure (SaO2<90% or partial oxygen pressure [pO2] <60 mmHg or Long-term O2 therapy heart failure (New York Heart Association class III-IV) prior CPAP therapy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco Campos-Rodriguez, MD
Organizational Affiliation
Sociedad Española de Neumología y Cirugía Torácica
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario Valme
City
Seville
ZIP/Postal Code
41014
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
31314107
Citation
Campos-Rodriguez F, Asensio-Cruz MI, Cordero-Guevara J, Jurado-Gamez B, Carmona-Bernal C, Gonzalez-Martinez M, Troncoso MF, Sanchez-Lopez V, Arellano-Orden E, Garcia-Sanchez MI, Martinez-Garcia MA; Spanish Sleep Network. Effect of continuous positive airway pressure on inflammatory, antioxidant, and depression biomarkers in women with obstructive sleep apnea: a randomized controlled trial. Sleep. 2019 Oct 9;42(10):zsz145. doi: 10.1093/sleep/zsz145.
Results Reference
derived
PubMed Identifier
28798089
Citation
Campos-Rodriguez F, Gonzalez-Martinez M, Sanchez-Armengol A, Jurado-Gamez B, Cordero-Guevara J, Reyes-Nunez N, Troncoso MF, Abad-Fernandez A, Teran-Santos J, Caballero-Rodriguez J, Martin-Romero M, Encabo-Motino A, Sacristan-Bou L, Navarro-Esteva J, Somoza-Gonzalez M, Masa JF, Sanchez-Quiroga MA, Jara-Chinarro B, Orosa-Bertol B, Martinez-Garcia MA; Spanish Sleep Network. Effect of continuous positive airway pressure on blood pressure and metabolic profile in women with sleep apnoea. Eur Respir J. 2017 Aug 10;50(2):1700257. doi: 10.1183/13993003.00257-2017. Print 2017 Aug.
Results Reference
derived
PubMed Identifier
27181196
Citation
Campos-Rodriguez F, Queipo-Corona C, Carmona-Bernal C, Jurado-Gamez B, Cordero-Guevara J, Reyes-Nunez N, Troncoso-Acevedo F, Abad-Fernandez A, Teran-Santos J, Caballero-Rodriguez J, Martin-Romero M, Encabo-Motino A, Sacristan-Bou L, Navarro-Esteva J, Somoza-Gonzalez M, Masa JF, Sanchez-Quiroga MA, Jara-Chinarro B, Orosa-Bertol B, Martinez-Garcia MA; Spanish Sleep Network. Continuous Positive Airway Pressure Improves Quality of Life in Women with Obstructive Sleep Apnea. A Randomized Controlled Trial. Am J Respir Crit Care Med. 2016 Nov 15;194(10):1286-1294. doi: 10.1164/rccm.201602-0265OC.
Results Reference
derived

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Effect of CPAP Treatment in Women With Moderate-to-severe OSA.

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