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Recruiting NCT06947174

NCT06947174 The Role of Angiographic Measurements and Anatomical Correlations in Intra-Aortic Balloon Pump (IABP) Size Selection

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Clinical Trial Summary
NCT ID NCT06947174
Status Recruiting
Phase
Sponsor Siriraj Hospital
Condition Intra-aortic Balloon Pump
Study Type OBSERVATIONAL
Enrollment 68 participants
Start Date 2025-01-25
Primary Completion 2025-11-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 68 participants in total. It began in 2025-01-25 with a primary completion date of 2025-11-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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).

Eligibility Criteria

Inclusion Criteria: * Patients had obtained CT scan of chest with upper abdomen with celiac trunk visualize within 1 year from the day of transfemoral angiography * Patients had who will undergo transfemoral angiography as clinical indicated * Patients had obtained Chest X-ray within 1 year from the day of transfemoral angiography Exclusion Criteria: * Patient with limb amputation * Patient with known aortic abnormalities such as aortic aneurysm, aortic dissection

Contact & Investigator

Central Contact

James Tisyakorn, Doctor of Medicine

✉ james51236@gmail.com

📞 +66925549747

Principal Investigator

Ploy Pengchata, Doctor of Medicine

PRINCIPAL INVESTIGATOR

Her Majesty Cardiac Center, Faculty of Medicine Siriraj Hospital

Frequently Asked Questions

Who can join the NCT06947174 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Intra-aortic Balloon Pump. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06947174 currently recruiting?

Yes, NCT06947174 is actively recruiting participants. Contact the research team at james51236@gmail.com for enrollment information.

Where is the NCT06947174 trial being conducted?

This trial is being conducted at Bangkok Noi, Thailand.

Who is sponsoring the NCT06947174 clinical trial?

NCT06947174 is sponsored by Siriraj Hospital. The principal investigator is Ploy Pengchata, Doctor of Medicine at Her Majesty Cardiac Center, Faculty of Medicine Siriraj Hospital. The trial plans to enroll 68 participants.

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