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Ultrasound-guided Pecto-Intercostal Fascial Plane Block for Chronic Postoperative Pain After Cardiac Surgery via Median Sternotomy: A Randomized Controlled Trial

Effect of Ultrasound-guided Pecto-Intercostal Fascial Plane Block on Chronic Postoperative Pain Incidence After Median Sternotomy for Cardiac Surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104378
Enrollment
Unknown
Registered
2025-06-16
Start date
2025-08-08
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Acute and chronic pain after median thoracotomy for cardiac surgery

Interventions

Pecto-Intercostal Fascial Plane Block(FIFP group):In the intervention group, a linear ultrasound transducer was positioned in the parasagittal plane between the fourth and fifth intercostal spaces, 2-
Control group:In the control group, a linear ultrasound transducer was positioned identically in the parasagittal plane between the fourth and fifth intercostal spaces, 2-3 cm lateral to the midline,

Sponsors

Zhongda Hospital, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are scheduled to undergo median thoracotomy for the first time; 2. Age >=18 years old; 4. American Society of Anesthesiologists (ASA) classification grades I-IV; 5. Patients who have been reviewed and approved by the ethics committee of this hospital and have signed a consent form with the patient or their family.

Exclusion criteria

Exclusion criteria: 1. Patients with relative or absolute contraindications to nerve block puncture: e.g., allergy to local anesthetics, infection or hematoma at the puncture site; 2. Pre-existing acute or chronic pain; 3. History of preoperative opioid use; 4. Severe systemic diseases (renal, hepatic, pulmonary, or endocrine); 5. Preoperative psychiatric disorders, communication barriers, or refusal to participate; 6. Patients requiring reoperation or postoperative death.

Design outcomes

Primary

MeasureTime frame
The incidence of chronic pain three months after the surgery;

Secondary

MeasureTime frame
Postoperative acute pain;The incidence of chronic pain at 6 months and 12 months after the surgery;Impact of chronic pain on quality of life, assessment of postoperative pain characteristics, and status of anxiety and depression at 3, 6, and 12 months postoperatively;Patient satisfaction with analgesia;Postoperative recovery quality;Total opioid consumption within 5 days after surgery;Adverse events related to thoracic intercostal fascial plane block;Incidence of nausea, vomiting, dizziness and pruritus within 48h;Time to first administration of rescue analgesics;Extubation time;Length of stay in ICU;Total length of stay;Drainage tube placement time;

Countries

China

Contacts

Public ContactJuan Yao

Department of Anesthesiology, Surgery and Pain Management, Zhong da Hospital, Southeast University

yaojuanmazui@163.com+86 159 5056 3770

Outcome results

None listed

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