Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
103 participants
INTERVENTIONAL
2007-12-31
2009-10-31
Brief Summary
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Our hypothesis is that we can increase heart rate by using atropin in these patients, so we will achieve more conclusive results.
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
SINGLE_GROUP
DIAGNOSTIC
NONE
Study Groups
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1
Pateints who achieve target haert rate or conclusive test will not be given Atropine
Atropine
I.V Atropine 0.5mg up to 2 mg
2
Patients who won't achieve tarhet heart rate or conclusive results will be given Atropine
Atropine
I.V Atropine 0.5mg up to 2 mg
Interventions
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Atropine
I.V Atropine 0.5mg up to 2 mg
Eligibility Criteria
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Inclusion Criteria
* Age\> 18 years old
Exclusion Criteria
* Patients with LBBB
* Unstable Angina
* Recent Myocardial Infarction
* Un controlled Arrythmia
* Congestive heart faliure
* Severe symptomatic valvular heart disease
* Acute Pulmonary Embolism
* Acute perimyocarditis
* Acute aortic dissection
Relative:
* Lt main stenosis
* Severe hypertention (Systolic\> 200 mmHg; Diastolic \> 100 mmHg)
* Cardiomyopathy
* Obstructiove abnormalities
* Psychiatric disorders
* High degree AV Block
18 Years
FEMALE
No
Sponsors
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HaEmek Medical Center, Israel
OTHER
Responsible Party
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Mohamed Jabaren
MD
Locations
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Heart Institute, Ha'Emek Medical Center
Afula, Afula, Israel
Countries
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Other Identifiers
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07-0139 EMC
Identifier Type: -
Identifier Source: org_study_id
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