- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06913595
Low Molecular Weight Heparin vs Direct Oral Anticoagulant After Bariatric Surgery
August 23, 2025 updated by: Mohammed Elshwadfy Nageeb, Cairo University
Extended Venous Thromboemboism Prophylaxis After Bariatric Surgeries: A Comparison Of Low Molecular Weight Heparin With Direct Oral Anticoagulant
Extended Venous Thromboemboism Prophylaxis After Bariatric Surgeries: A Comparison Of Low Molecular Weight Heparin With Direct Oral Anticoagulant
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
This study aims to compare the effectiveness of rivaroxaban versus low molecular weight heparin in reducing the incidence of PMVT after bariatric surgery.
Study Type
Interventional
Enrollment (Estimated)
100
Phase
- Phase 1
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt, 11511
- Cairo University
-
-
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
No
Description
Inclusion Criteria:
- BARIATRIC PATIENTS
Exclusion Criteria:
- BLEEDING TENDENCY
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
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Low Molecular Weight Heparin
Low molecular weight heparin as aprophylaxis after bariatric surgery
|
Low molecular weight heparin after bariatric surgery
Other Names:
|
|
Experimental: Direct Oral Anticoagulant.
Direct Oral Anticoagulant as aprophylaxis after bariatric surgery
|
Direct Oral Anticoagulant AFTER BARIATRIC SURGERY
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
VENOUS THROMBOEMBOLISM
Time Frame: 1 year
|
DVT after bariatric surgery
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: mohammed elshwadfy, Cairo University
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)
March 25, 2024
Primary Completion (Estimated)
October 25, 2025
Study Completion (Estimated)
November 1, 2025
Study Registration Dates
First Submitted
March 24, 2025
First Submitted That Met QC Criteria
April 3, 2025
First Posted (Actual)
April 6, 2025
Study Record Updates
Last Update Posted (Estimated)
August 26, 2025
Last Update Submitted That Met QC Criteria
August 23, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- N-55-2024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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