Comparison of the effect of oxygen and placebo in treatment of non ST elevation acute coronary syndrome
Not Applicable
- Conditions
- Ischaemic heart diseases.????? ????????? ????????? ??? ??????? ??? ????????I20.0, I21
- Registration Number
- IRCT2014081118768N1
- Lead Sponsor
- Research Deputy of Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
Age between 18-84 years; diagnosed with acute coronary syndrome with non ST segment elevation according to Branvald criteria; no clinical evidence of heart failure; no chronic lung disease or other respiratory problems; lack of cardiac arrest or cardiogenic shock before entering the hospital; oxygen saturation above 90% on admission; absence of congenital heart disease.
Exclusion criteria: Need for inotropic support; having ST elevation acute myocardial infarction; oxygen saturation less than 90% during hospitalization; emergency coronary angioplasty or emergency coronary artery bypass during hospitalization; death.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cardiac dysrhythmias. Timepoint: Continues over 24 hours. Method of measurement: Cardiac monitoring device.;Chest pain. Timepoint: 24 - 28 - 32 - 36 - 40 - 44 - 48 hours. Method of measurement: check list, visual analogue scale.;The amount of narcotic analgesic. Timepoint: 48 hours. Method of measurement: check list.
- Secondary Outcome Measures
Name Time Method Readmission due to cardiac problems. Timepoint: End of weeks 1- 2- 3- 4. Method of measurement: The phone call.;Visit due to cardiac problems. Timepoint: End of weeks 1- 2- 3- 4. Method of measurement: The phone call.