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Myocardialbridge Bypass Graft Surgery Efficacy Verification

Myocardialbridge Bypass Graft Surgery Efficacy Verification

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06857838
Enrollment
500
Registered
2025-03-04
Start date
2020-01-01
Completion date
2040-12-31
Last updated
2025-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Brief 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.

Interventions

PROCEDUREMBBG

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.

PROCEDUREMB 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.

PROCEDUREMB 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

Xi'an International Medical Center Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with myocardialbridge requiring drug therapy or surgical intervention.

Exclusion criteria

* patients with myocardialbridge not requiring drug therapy or surgical intervention, or unwilling to be enrolled for any reason

Design outcomes

Primary

MeasureTime frame
All-Cause MortalityUp to 240 months
Rate of counduit patencyUp to 180 months

Countries

China

Contacts

Primary ContactZhen Wang, Doctorate
wang.zhen@000516.cn+86-029-68302464
Backup ContactJinzhou Zhang, Doctorate
zhang.jinzhou@000516.cn+86-029-68302464

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026