Myocardialbridge Bypass Graft Surgery Efficacy Verification

NCT06857838 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 500

Last updated 2025-03-04

No results posted yet for this study

Summary

Myocardial Bridge Bypass Graft surgery is introduced to relieve the unmedical symptoms of patients with long-segment or deep myocardial bridge, clinical outcomes will be collected to verify the effectiveness of the surgery.

Conditions

  • Myocardial Bridge of Coronary Artery
  • Myocardial Bridge
  • Myocardial Bridging
  • Myocardial Infarction
  • Myocardial Ischemia
  • Pectoris, Stable Angina
  • Sudden Cardiac Death
  • Bypass Graft Stenosis
  • Bypass Graft Occlusion
  • Bypass Graft Thrombosis

Interventions

PROCEDURE

MBBG

The patients with deep(depth\>2mm) and long-segement(length\>25mm) of myocardialbridge receiving myocardialbridge bypass graft surgery(MBBG),fulfilling the following criteria: 1.presenting with pectoris angina that cannot be effectively relieved by maximum guideline-directed drug therapy; 2. No atherosclerotic plaque or merely mild atherosclerotic stenosis is detected at the proximal or entry of the myocardialbridge confirmed by coronory artery angiography.

PROCEDURE

MB CABG

The patients with deep(depth\>2mm) and long-segement(length\>25mm) of myocardialbridge receiving myocardialbridge bypass graft surgery(MBBG),fulfilling the following criteria: 1.presenting with pectoris angina that cannot be effectively relieved by maximum guideline-directed drug therapy; 2. The moderate-to-severe atherosclerotic stenosis is detected at the proximal or entry of the myocardialbridge confirmed by coronory artery angiography.

PROCEDURE

MB unroof

The patients with superficial type(depth\<2mm) and short-segement(length\<25mm) of myocardial bridge will be allocated to receive myocardialbridge "unroof" surgery,when fulfilling the following criteria: 1.presenting with pectoris angina that cannot be effectively relieved by maximum guideline-directed drug therapy; 2. The MB was superficial and short confirmed by coronory artery CT angiography.

Sponsors & Collaborators

  • Xi'an International Medical Center Hospital

    lead OTHER

Principal Investigators

  • Zhen Wang, Doctorate · Xi'an International Medical Center Hospital Affiliated To Northwest University

  • Jinzhou Zhang, Doctorate · Xi'an International Medical Center Hospital Affiliated To Northwest University

  • Jinzhou Zhang, Doctorate · Xi'an International Medical Center Hospital Affiliated To Northwest University

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-01
Primary Completion
2030-12-31
Completion
2040-12-31

Countries

  • China

Study Locations

More Related Trials

Entities

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 NCT06857838 on ClinicalTrials.gov