Effect of Increased Oxygenation in the Air During Endurance Training in Stable Angina Pectoris Patients
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ClinicalTrials.gov Identifier: NCT00184444 |
Recruitment Status :
Completed
First Posted : September 16, 2005
Last Update Posted : July 20, 2016
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The study investigates whether endurance training breathing 100% oxygen gives a additional improvement of maximal oxygen uptake in stable Angina Pectoris patients, compared to training without extra oxygen supplementation. In addition work economy, stroke volume and cardiac perfusion is measured.
The hypothesis of the study is that increased oxygenation of the air increases performance, stroke volume, work economy and cardiac perfusion.
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Angina Pectoris | Behavioral: Hypoxic interval training Behavioral: Normoxic interval training | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 25 participants |
Allocation: | Non-Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Effect of Increased Oxygenation in the Air During Endurance Training in Stable Angina Pectoris Patients |
Study Start Date : | September 2004 |
Actual Primary Completion Date : | July 2007 |
Actual Study Completion Date : | July 2007 |
Arm | Intervention/treatment |
---|---|
Experimental: Hypoxic Interval training
4 x 4 minutes interval training with 100% oxygenated air
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Behavioral: Hypoxic interval training
4 x 4 minutes interval training in hypoxic air, 3 times per week at 90-95% HR max |
Experimental: Normoxic interval training
4 x 4 minutes interval training in normoxic air
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Behavioral: Normoxic interval training
4 x 4 minutes normoxic interval training, 3 times per week at 90-95% HR max |
- maximal oxygen uptake [ Time Frame: Baseline and post training ]
- Cardiac perfusion [ Time Frame: Baseline and post training ]
- work economy [ Time Frame: Baseline and post training ]
- cardiac output [ Time Frame: baseline and post training ]

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Ages Eligible for Study: | 18 Years to 75 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- stable angina pectoris age 18-75
Exclusion Criteria:
- unstable angina pectoris
- Limitations to exercise other than coronary artery disease
- Participants in other study interventions

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00184444
Norway | |
Norwegian University of Science and Technology | |
Trondheim, Norway, 7489 |
Study Director: | Asbjørn Støylen, MD | Norwegian university of sience and technology |
Responsible Party: | Norwegian University of Science and Technology |
ClinicalTrials.gov Identifier: | NCT00184444 |
Other Study ID Numbers: |
094-2004 |
First Posted: | September 16, 2005 Key Record Dates |
Last Update Posted: | July 20, 2016 |
Last Verified: | July 2016 |
angina pectoris hyperoxia endurance training stroke volume cardiac perfusion |
Angina Pectoris Angina, Stable Myocardial Ischemia Heart Diseases Cardiovascular Diseases |
Vascular Diseases Chest Pain Pain Neurologic Manifestations |