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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01621061
Other study ID # 01-7/219
Secondary ID
Status Completed
Phase N/A
First received June 13, 2012
Last updated May 14, 2014
Start date June 2012
Est. completion date December 2013

Study information

Verified date May 2014
Source University of Zurich
Contact n/a
Is FDA regulated No
Health authority Kyrgyzstan: Research Ethics Committee
Study type Observational

Clinical Trial Summary

High altitude pulmonary hypertension, a form of altitude illness that occurs in long-term residents at altitudes >2500 m, is characterized by dyspnea, hypoxemia, impaired exercise performance and hypertension in the pulmonary circulation. Whether sleep related breathing disturbances, common causes of nocturnal hypoxemia in lowlanders, are also prevalent in highlanders and promote pulmonary hypertension in highlanders is unknown. Therefore, the current study will investigate whether highlanders with high altitude pulmonary hypertension have a greater prevalence of sleep apnea than healthy highlanders and lowlanders.


Recruitment information / eligibility

Status Completed
Enrollment 125
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 16 Years and older
Eligibility Inclusion Criteria:

- high altitude pulmonary hypertension confirmed by clinical presentation and systolic pulmonary artery pressure >50 mmHg measured by echocardiography at altitude of residence.

- healthy subjects (high altitude controls)

- Both genders

- Age >16 y

- Kyrgyz ethnicity

- born, raised and currently living at >2500 m

- healthy subjects currently living at <1000 m (low altitude controls)

Exclusion criteria:

- Pulmonary hypertension from other causes, in particular from left ventricular failure as judged clinically and by echocardiography

- excessive erythrocytosis

- other coexistent disorders that may interfere with the cardio-respiratory system and sleep

- regular use of medication that affects control of breathing

- heavy smoking

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Kyrgyzstan National Center for Cardiology and Internal Medicine Bishkek

Sponsors (2)

Lead Sponsor Collaborator
University of Zurich National Center of Cardiology and Internal Medicine, Kyrgyzstan

Country where clinical trial is conducted

Kyrgyzstan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Sleep related breathing disturbances Nocturnal oxygen saturation and apnea/hypopnea index 4 months No
Secondary Pulmonary artery pressure Echocardiography 4 months No
Secondary Dyspnea NYHA functional class 4 months No
Secondary Vigilance Psychomotor vigilance 4 months No
Secondary Exercise performance 6 min walk test 4 months No
Secondary Pulmonary function Spirometry 4 months No
Secondary Cerebral oxygen saturation Near-infrared spectroscopy 4 months No
Secondary Mountain sickness Quinghai chronic mountain sickness score 4 months No
Secondary Generic quality of life SF-36 quality of life questionnaire 4 months No
Secondary Disease specific quality of life Kansas City Cardiomyopathy questionnaire 4 months No
Secondary Subjective sleepiness Epworth sleepiness scale 4 months No
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