The Role of Angiographic Measurements and Anatomical Correlations in Intra-Aortic Balloon Pump (IABP) Size Selection

NCT06947174 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 68

Last updated 2025-04-27

No results posted yet for this study

Summary

The goal of this study aim to accurately size the IABP size for patients. The main questions it aims to answer are:

* Are patients's height, jugular notch to transpyloric plane distance and distance from the carina to the upper part of the first lumbar vertebra (measured by chest X-ray) are a good surrogate for IABP sizing?
* Is the distance obtained during a transfemoral artery catheterization a reliable way to size the IABP? Researchers will enroll patient who have had previous CT that include thoracic aorta to celiac trunk who will undergo transfemoral angiography.
* All patients that researcher enrolled will undergo transfemoral angiography, during which the researchers will measure the vessel distance using a wire after the procedure end.
* Researchers will measure the height weight, jugular notch to transpyloric plane distance, CXR distance from carina to upper border of L1 and the distance from aorta at subclavian level to celiac trunk from CT.
* Researchers will find the correlation between of each measurement to the distance from aorta at subclavian level to celiac trunk from CT (considered the standard measure).

Conditions

  • Intra-aortic Balloon Pump

Sponsors & Collaborators

  • Siriraj Hospital

    lead OTHER

Principal Investigators

  • Ploy Pengchata, Doctor of Medicine · Her Majesty Cardiac Center, Faculty of Medicine Siriraj Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-01-25
Primary Completion
2025-11-30
Completion
2025-12-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06947174 on ClinicalTrials.gov