- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06691451
Inherited Thromophilia and Thrombotic Risks in Inflammatory Bowel Disease During Activity and Remission
November 14, 2024 updated by: Asmaa mohammed abdelaal abdelaal
Inherited Thrombophilia and Thrombotic Risks in Inflammatory Bowel Disease During Activity and Remission
Inherited thombopllia and thrombotic risks in inflammatory bowel Disease during activity and remission
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
Inflammatory bowel diseases (IBD) are systemic conditions characterized by multiple intestinal and extra-intestinal manifestations related to the associated chronic inflammatory state.
Among their diverse extra-intestinal complications, venous thromboembolism (VTE) remains one of the most under recognized causes of morbidity and mortality in these patients, highlighting the need for a better understanding of the underlying mechanism of hypercoagulability, in addition to the role of acquired and inherited risk factors that further increase the risk of thrombosis with its impact on patients' outcomes.[1,
2]
Study Type
Observational
Enrollment (Estimated)
93
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: Asmaa Mohammed Abdelaal, Master
- Phone Number: 01066239562 01066239562
- Email: Asmaamohammedabdelaal0098@gmail.com
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Study will be conducted at internal medicine department Assiut universty
Description
Inclusion Criteria:
- Age (18yrs - 65yrs) both sex
Exclusion Criteria:
- Presence of acquired cause (pregnancy, recent surgery, history of drug, History of malignant Disease, History of blood or blood product transfusion in last 4 weeks)
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Comparison between the number of IBD patients with tendency to thrombosis in cases of activity-
Time Frame: Baseline
|
-investigate the presence of multiple mutations associated with IBD patients with or without vascular complications.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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 (Estimated)
November 1, 2024
Primary Completion (Estimated)
December 1, 2026
Study Completion (Estimated)
March 1, 2027
Study Registration Dates
First Submitted
November 14, 2024
First Submitted That Met QC Criteria
November 14, 2024
First Posted (Actual)
November 15, 2024
Study Record Updates
Last Update Posted (Actual)
November 15, 2024
Last Update Submitted That Met QC Criteria
November 14, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Thrombophilia in ibd patients
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.