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A single-center, prospective, randomized, controlled study on perioperative analgesic effect of transverse thoracic muscle plane block on patients undergoing coronary artery bypass grafting surgery

A single-center, prospective, randomized, controlled study on perioperative analgesic effect of transverse thoracic muscle plane block on patients undergoing coronary artery bypass grafting surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030079
Enrollment
Unknown
Registered
2020-02-22
Start date
2020-03-01
Completion date
Unknown
Last updated
2021-05-10

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

Conditions

Coronary heart disease

Interventions

contrast group:no nerve block,postoperative PCVA
3/4 group:TTPB in the 3/4 intercostal space, the same PCVA as C group
4/5 group:TTPB in the 4/5 intercostal space, the same PCVA as C group

Sponsors

The First Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged >= 18 years; 2. Preoperative color Doppler ultrasound: M-mode ultrasound Teichholz method to measure left ventricular ejection fraction >= 50%; 3. Elective open CABG surgery under CPB; 4. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Have contraindications to nerve block; 2. Have a history of cardiac surgery; 3. Need ventricular assist devices such as IABP to assist circulation before surgery; 4. Have a history of cardiac arrest; 5. Have cognitive dysfunction.

Design outcomes

Primary

MeasureTime frame
Intraoperative opioid consumption;Cool sansation block range;Range of decreased mechanical pain;

Secondary

MeasureTime frame
Postoperative mechanical ventilation time;ICU stay;Postoperative hospital stay;nausea and vomitting;Short-term myocardial injury markers after surgery;Heart rate (bpm) and blood pressure (mmHg) fluctuate to the maximum value during operative stimulation;Consumption of vasoactive agents or antihypertensive drugs intraoperatively;NRS pain score at 1.2.3.5.7 days after surgery;

Countries

China

Contacts

Public ContactYu Chen

The First Affiliated Hospital affiliated to Sun Yat-Sen University

aruhan0123@outlook.com+86 13631453324

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026