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NCT06934993Completed

Comparison of Bidirectional Palpation Test and Transit Time Flow Measurement for LIMA-LAD Graft Patency

Source: ClinicalTrials.gov · Last updated 8 Jul 2025

Brief summary (registry, in English)

The most important factor determining mortality and morbidity after coronary artery bypass graft (CABG) surgery is graft patency. The LIMA-LAD anastomosis is the most crucial anastomosis because it's revascularizing the most important and large region of the heart, has superior long-term graft patency rates and is considered the gold standard for CABG. Therefore, ensuring the patency of the LIMA-LAD anastomosis is vital for both early and late outcomes. The bidirectional palpation test (BPT), developed in our clinic to assess graft patency, is a subjective test, yet it is simple and reliable. Additionally, transit time flow meter (TTFM) measurements have also been performed. In this study, the efficacy of BPT and the results of TTFM measurements were compared by examining graft patency through early-period coronary CT angiography (CCTA).

Status (registry)
Completed
Study type
Observational
Enrollment
116 (actual)
First submitted
11 Apr 2025
Start date
31 Aug 2023
Primary completion date
27 Aug 2024
Lead sponsor
Abdulgani Orhun YENİGÜN
NCT number
NCT06934993

What you commit to

  • Study type: Observational
  • Participants enrolled: 116
  • From 31 Aug 2023 to the primary completion date, 27 Aug 2024
  • 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.

Other illness

  • Patients in whom CT angiography is not appropriate: Such as acute or chronic renal failure

Lab values

  • Inability to Perform CABG: Patients for whom CABG could not be performed due to postoperative complications (e.g., elevated creatinine levels leading to inability to perform CABG, 43 patients).

Other

  • Refusal to Participate: Patients who did not wish to participate in the study after being approached.
  • Death in Early Postoperative Period: Patients who died in the early postoperative period (3 patients).

Who the study is looking for

  • Elective Isolated CABG Surgery: Patients undergoing elective isolated coronary artery bypass grafting (CABG).
  • CABG with Additional Cardiac Surgery: Patients who had CABG surgery in conjunction with other cardiac procedures.
  • Informed Consent: Patients who provided informed consent to participate in the study.
  • Postoperative Follow-Up: Patients who were followed up postoperatively and completed the necessary evaluations.
  • CABG patients whose renal functions are suitable for CTA

Age in the registry: 41 years to 81 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Istanbul University Cerrahpaşa - Cerrahpaşa Faculty of Medicine
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.