NCT06795308Not yet recruiting
The Effect of Position on Pain, Bleeding, Hematoma and Vital Signs After Transfemoral Coronary Angiography
Source: ClinicalTrials.gov · Last updated 5 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
In this study, it was aimed to determine the effect of the special position given to the patient after transfemoral coronary angiography (supine position that varies depending on the angles) on pain, bleeding, hematoma and vital signs.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 5 Dec 2024
- Start date
- 3 Feb 2025
- Primary completion date
- 30 May 2025
- Lead sponsor
- Mersin University
- Diseases
- Coronary artery disease
- NCT number
- NCT06795308
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 3 Feb 2025 to the primary completion date, 30 May 2025
- 1 site 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.
Prior treatment
- Previously treated with streptokinase
- Those who have had back surgery/herniated disc,
Other illness
- Those with active hemorrhage
Other
- People with hemophilia or other coagulation defects
- Using more than 2 anticoagulants or antiplatelets
- Having chronic waist, back or leg pain
- Using any of the complementary and integrated methods
- Do not use any analgesic before, during and after transfemoral angiography.
- Radial angiography procedure was performed
- Patients coming to the service with sandbags
- Those who had any health problems or lost their lives during the application process
- Those who cannot continue the research for any reason
- Patients who wish to leave the study with their own consent
Who the study is looking for
- Written and verbal permission was obtained to participate in the research.
- Able to read, write, speak and understand Turkish
- Those who are over 18 years old
- Planned transfemoral angiography was performed
- Having normal prothrombin time (PT) and international normalization ratio (INR)
- Being conscious, fully oriented and cooperative, and open to communication.
- Those whose general condition is good and comfortable (vital signs are within normal limits)
- Not using any sedative medication,
- Those who have not previously had widespread hemorrhage, large hematoma, or a pain sensation greater than 4.5 on the visual pain scale
- Patients with imaging, medical treatment, stents, balloons, stents and balloons as a result of the procedure
- Not having any psychiatric disease
Age in the registry: 18 hours to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Adana City Training and Research Hospital Coordinator of this site? Confirm its status | Adana | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.