- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03310437
Cost Effectiveness if Primary PCI Versus Thrombolytic Therapy in Acute STEMI in Assiut University Hospital
July 1, 2019 updated by: Nahed Sameh Zaki
Cost Effectiveness of Primary PCI Versus Thrombolytic Therapy in STEMI in Assiut University Hospital
Cost effectiveness between PPCI and thrombolytic therapy in STEMI patients without contraindications
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Cost effectiveness between PPCI and thrombolytic therapy in STEMI patients 100 patient each within 90 m for PPCI and 6h for thrombolytic
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nahed Sameh
- Phone Number: 01224721313
- Email: nahedsameh74@gmail.com
Study Locations
-
-
-
Assiut, Egypt
- Recruiting
- Assiut medicine faculty
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients presented by ST elevation myocardial infarction
Description
Inclusion Criteria:
- All PPCI patients within 90 minutes door to ballon.
- All thrombolytic patient without contraindication ,within 6 golden hours of chest pain.
Exclusion Criteria:
- patients don't meet inclusion criteria
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Primary PCI
In primary PCI we use arterial sheath , wires ,heparin ,intracoronary stents
|
Primary percutaneous coronary intervention in acute myocardial infarction patients
|
Thrombolytic
In patients recieving thrombolytics they continue on LWMH for 72h ,plus aspirin , clopedogril , BB, statins
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Compare between PPCI and thrombolytic therapy regarding over all cost in STEMI patients
Time Frame: one year for collecting 100 patient for each arm with follow up 6 month
|
we will compare different outcomes in ST elevation myocardial infarction patients presented to our hospital who had recieved intervention (primary PCI ) versus thrombolytic as regarded in all over cost in egyptian pounds and follow up for 6 month
|
one year for collecting 100 patient for each arm with follow up 6 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 7, 2018
Primary Completion (Anticipated)
April 1, 2020
Study Completion (Anticipated)
October 1, 2020
Study Registration Dates
First Submitted
September 25, 2017
First Submitted That Met QC Criteria
October 10, 2017
First Posted (Actual)
October 16, 2017
Study Record Updates
Last Update Posted (Actual)
July 5, 2019
Last Update Submitted That Met QC Criteria
July 1, 2019
Last Verified
July 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 81
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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