Actively Recruiting
Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Endovascular Cardiac Interventions
Led by Istanbul University - Cerrahpasa · Updated on 2026-05-08
100
Participants Needed
1
Research Sites
118 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Sensory innervation of the femoral region which is the entry point for endovascular cardiac interventions such as coronary angiography,cardiac catheterization and percutaneous coronary intervention is complex.It is thought that the ilioinguinal and iliohypogastric nerves contribute mostly.With transversus abdominis plane block(TAPB),it is planned to provide analgesia by creating a block in these nerve branches that contribute to the sensory innervation of the intervention area.In addition;it was aimed to investigate patient's and physician's satisfaction during the procedure.
CONDITIONS
Official Title
Ultrasound-Guided Transversus Abdominis Plan (TAP) Block in Endovascular Cardiac Interventions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The patient is over 18 years of age
- Coronary angiography, cardiac catheterization and percutaneous coronary intervention will be applied to the patient
- The above-mentioned procedures will be taken under elective conditions
- Providing an optimal image when imaging the patient with ultrasound
- INR < 1.5
- If the patient gives consent, S/he will be included in the study.
You will not qualify if you...
- Patients under 18 years of age
- Patients treated under emergency conditions
- Morbid obesity (BMI >35 kg/m2)
- Pregnant women
- New York Heart Association (NYHA) stage 4 patients with advanced decompensated heart failure
- Patients with symptoms such as redness, temperature increase, infection, hematoma in the application area before the procedure
- Patients with a history of allergy to local anesthetics
- Patients who cannot be communicated
- Those with severe psychosis or progressive neurological deficits and muscle disease
- Patients who do not consent to the application will be excluded from the study.
AI-Screening
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Trial Site Locations
Total: 1 location
1
Istanbul University- Cerrahpasa
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
G
Gozde Altun
CONTACT
K
Kerem Erkalp
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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