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Clinical study of ultrasound-guided intercostal nerve anterior cutaneous branch block technique

Clinical study of ultrasound-guided intercostal nerve anterior cutaneous branch block technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100288
Enrollment
Unknown
Registered
2025-04-07
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

heart failure

Interventions

Control group:Conventional intravenous analgesia combined with tracheal intubation general anesthesia.
TTMP group:Ultrasound-guided bilateral transverse thoracic muscle plane block
PIFB group:Ultrasound-guided pectoralis major intercostal muscle plane block group

Sponsors

The first affiliated hostipal of nanchang university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective open heart surgery; 2.Aged 18-75 years, male or female; 3. ASA class II ~ III, NYHA class II ~ III; 4.There was no serious liver, lung and kidney disease; 5.Patients who can be followed up regularly according to the time required for this study;

Exclusion criteria

Exclusion criteria: 1.Poor general condition or severe liver, lung and kidney diseases; 2. Allergic to ropivacaine; 3.TTMP block and PIFB puncture site infection; 4.Patients with chest deformity who could not undergo TTMP block and PIFB; 5.Operations lasting more than 6 hours; 6.The life expectancy is no more than 3 months. 7.Have a history of mental illness or cognitive dysfunction; 8.Patients who cannot be followed up on time according to the requirements of the study;

Design outcomes

Primary

MeasureTime frame
visual analogue scale;Nerve block plane;puncturetime;Minimum Mental State Examination score;

Secondary

MeasureTime frame
Tracheal intubation removal time;Postoperative independent standing time;Sufentanil, remifentanil, propofol dosage;Drainage tube removal time;Incidence of postoperative nausea and vomiting;Retention time in intensive care unit;Intraoperative cyclic fluctuations;Postoperative analgesic drug dose;

Countries

China

Contacts

Public ContactYang Zhang

The first affiliated hostipal of nanchang university

mzzhangyang@126.com+86 13576080494

Outcome results

None listed

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