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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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24 May 2021 |
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Main ID: |
NCT03209622 |
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Date of registration:
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20/06/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Smoking Cessation After Acute Coronary Syndrome
SCACS |
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Scientific title:
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Nicotine Replacement Therapy After Acute Coronary Syndrome |
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Date of first enrolment:
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January 2, 2015 |
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Target sample size:
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89 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03209622 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: None (Open Label).
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Phase:
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N/A
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Countries of recruitment
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Tunisia
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Contacts
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Name:
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Aymen Elhraiech, A. professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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University hospital of Monastir: Avenue Farhat HACHED 5000 Monastir Tunisia |
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Name:
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Asma Sriha Belguith, Professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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University hospital of Monastir: Avenue Farhat HACHED 5000 Monastir Tunisia |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- patients aged more than 18 years, hospitalized with an ACS actively smoking at the
time of inclusion, motivated to quit smoking, able to provide informed consent and
willing to participate in a clinical study including a follow-up examination every 2
weeks after hospital discharge.
Exclusion Criteria:
- the refusal of assistance of smoking cessation, inability to follow-up clinical visit
(professional, regional or physical hindrance), diagnosis of depression or of serious
health condition at admission (ventilated patient, cardiogenic shock, etc).
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Male
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Health Condition(s) or Problem(s) studied
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Acute Coronary Syndrome
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Recurrence
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Smoking
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Intervention(s)
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Drug: Nicotine patch
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Procedure: Nicotine replacement therapy delivred in cardiology intensive care unit versus Nicotine replacement therapy delivered after hospital discharge
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Other: the external consultation
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Primary Outcome(s)
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smoking cessation rates with NRT among patients hospitalized for acute coronary syndrome
[Time Frame: 24 weeks after acute coronary syndrome]
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Secondary Outcome(s)
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smoking cessation duration with NRT among patients hospitalized for acute coronary syndrome
[Time Frame: 24 weeks after acute coronary syndrome]
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Secondary ID(s)
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PMEMonastir
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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