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Comparison of the analgesic effects of ultrasound-guided paraspinal, erector and transverse pectoral muscle block in patients undergoing cardiac surgery

Comparison of the analgesic effects of ultrasound-guided paraspinal, erector and transverse pectoral muscle block in patients undergoing cardiac surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093387
Enrollment
Unknown
Registered
2024-12-03
Start date
2023-11-09
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

valvular heart disease

Interventions

PVB Group:Paravertebral nerve block was performed in bilateral T2-3 and T4-5 spaces under ultrasound guidance with 0.4% Ropivacaine and 14 mg compound betamethasone at each injection point followed by
ESPB Group:At first, 0.4% Ropivacaine and 14 mg compound betamethasone were injected into each injection site with 20 ml of drugs, then general anesthesia was performed.
TTMPB Group:Transthoracic muscle block was performed at bilateral T3-T4 intercostal space under ultrasound guidance. 0.4% ropivacaine and 14 mg compound betamethasone was injected into each injection

Sponsors

The Second Xiangya Hospital of Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged over 18 years; 2. Elective cardiac valve surgery with cardiopulmonary bypass 3. ASA grade II-III; 4. New York Heart Association class II-III; 5. First Heart Surgery 6. Sign the informed consent form voluntarily.

Exclusion criteria

Exclusion criteria: 1. Contraindications to nerve block, including anatomical variations of the puncture site due to infection, tumor, or severe deformity, Coagulopathy, allergy to local anesthetics, etc. 2. History of chronic pain or opioid abuse 3. Mental Illness 4. Use of analgesics before surgery 5. Liver and kidney dysfunction 6. Others are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Amount of sufentanil used during operation;NRS scores at rest and cough at 24h and 48 h after operation;The Times of rescue analgesia within 24 h and 48 h after operation;

Secondary

MeasureTime frame
Duration of mechanical ventilation;Length of stay in the ICU;Length of hospital stay;

Countries

China

Contacts

Public ContactXu Junmei

The Second Xiangya Hospital of Central South University

13975148864@139.com+86 139 7514 8864

Outcome results

None listed

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