NCT05501964Completed
Predictors and Outcomes of Time to Hemostasis After Cardiac Catheterization
Predictors and Outcomes of Time to Hemostasis Post Trans-femoral Cardiac Catheterization: a Multicenter Cohort Study
Source: ClinicalTrials.gov · Last updated 26 Jun 2024
Brief summary (registry, in English)
This study aims to: 1. Assess the incidence of hemostasis failure after manual compression of trans-femoral arterial sheath post percutaneous coronary intervention. 2. Assess the predictors of time to hemostasis achieved by manual compression for trans-femoral arterial sheath post percutaneous coronary intervention. 3. Assess the association between time to hemostasis and the incidence of vascular access complications after manual compression for trans-femoral arterial sheath removal post percutaneous coronary intervention. 4. Assess the association between failed hemostasis and the incidence of vascular access complications after manual compression for trans-femoral arterial sheath removal post percutaneous coronary intervention.
- Status (registry)
- Completed
- Study type
- Observational
- Enrollment
- 300 (actual)
- First submitted
- 6 Aug 2022
- Start date
- Aug 2022
- Primary completion date
- May 2024
- Lead sponsor
- Alexandria University
- Diseases
- Coronary artery disease
- NCT number
- NCT05501964
What you commit to
- Study type: Observational
- Participants enrolled: 300
- From Aug 2022 to the primary completion date, May 2024
- 5 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- patients with a known history of coagulation disorders,
Lab values
- patients with sheath removed at the laboratory, and
Other
- Patients who had trans-femoral catheterization procedure within a 1-month duration
- Patients who experience post - catheterization life-threatening events rather than vascular access complications
Who the study is looking for
- Patients who planned for elective or primary percutaneous coronary intervention with femoral access, and
- Agreed to participate in the study
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (5)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Mabaret Aalsafra hospital Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
| Smouha University hospital Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
| Shark El-Madina Hospital Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
| Andalusia Private Hospital Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
| German Heart Center Coordinator of this site? Confirm its status | Alexandria | Egypt | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.