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Effect of bilateral transversus thoracis muscle plane block on postoperative recovery quality and analgesic effect in patients undergoing cardiac surgery via median sternotomy

Effect of bilateral transversus thoracis muscle plane block on postoperative recovery quality and analgesic effect in patients undergoing cardiac surgery via median sternotomy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062390
Enrollment
Unknown
Registered
2022-08-04
Start date
2022-08-03
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

heart disease

Interventions

The transversus thoracis muscle plane block group:The bilateral transversus thoracis muscle plane block
Control group:No intervention

Sponsors

The second Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective midsternal cardiac surgery; 2. Age 18-65, both sexes; 3. ASA classification ?-?, NYHA classification ?-?; 4. Volunteer to join and sign informed consent after fully explaining the content of the clinical trial.

Exclusion criteria

Exclusion criteria: 1. The patient refused to participate; 2. Coagulopathy or infection at the puncture site; 3. Previous local anesthetic allergy; 4. Patients with chronic pain and long-term oral analgesics; 5. Complicated with serious diseases, such as abnormal liver and kidney function and lung function; 6. Poor control of diabetes and hypertension; 7. Patients undergoing emergency or secondary surgery; 8. People with severe mental illness or difficulty communicating.

Design outcomes

Primary

MeasureTime frame
QOR-40 score;

Secondary

MeasureTime frame
Postoperative pain scale;Opioid consumption;Time of first remedial analgesia;Inflammatory factor;Cardiac troponin I;Incidence of adverse reactions within 48 hours;Duration of mechanical ventilation;Incidence of pulmonary complications within 7 days after operation;ICU length of stay;Exhaust and defecation time;Postoperative activity time;Incidence of chronic pain;

Countries

China

Contacts

Public ContactYun Li
yunli_001@aliyun.com+86 15105517565

Outcome results

None listed

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