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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00718406
Other study ID # S203-02
Secondary ID
Status Completed
Phase Phase 4
First received July 16, 2008
Last updated July 16, 2008

Study information

Verified date August 2002
Source Sahlgrenska University Hospital, Sweden
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

The primary aim was to evaluate the relief of chest pain during the first 30 minutes among patients who received metoprolol alone as compared with metoprolol plus morphine


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Acute chest pain

- ECG-signs indicating myocardial ischemia

Exclusion Criteria:

- Heart rate < 60 beats/min

- Systolic blood pressure < 110 mmHg

- High degree AV-block

- Signs of obstructive pulmonary disease

- Signs of pulmonary oedema

- Unwillingness

- Participation in other studies

- Long delay between arrival of ambulance and randomisation

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Drug:
Metoprolol

metoprolol plus morphine


Locations

Country Name City State
Sweden Medical Institution, Dept of Molecular and Clinical Medicine, Sahlgrenska University Hospital Göteborg

Sponsors (2)

Lead Sponsor Collaborator
Sahlgrenska University Hospital, Sweden AstraZeneca

Country where clinical trial is conducted

Sweden, 

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