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Effect of Ultrasound-guided Pectoral Interfascial Plane Type I and Type II Blocks Combined with Local Anesthesia on Early Postoperative Pain After Minimally Invasive Breast Rotational Excision: A Retrospective Cohort Study

Effect of Ultrasound-guided Pectoral Interfascial Plane Type I and Type II Blocks Combined with Local Anesthesia on Early Postoperative Pain After Minimally Invasive Breast Rotational Excision: A Retrospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119569
Enrollment
Unknown
Registered
2026-02-28
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

breast lesion

Interventions

Pecs block group:None

Sponsors

Shenshan Central Hospital, Sun Yat-sen Memorial Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18–75 years old; 2. Diagnosed with breast nodules and scheduled for minimally invasive breast resection surgery; 3. American Society of Anesthesiologists (ASA) physical condition classification: I–III; 4. Surgery date between May 1, 2025 and November 30, 2025; 5. Complete preoperative assessment records, intraoperative anesthesia operation records, and 24-hour postoperative follow-up data; 6. Complete postoperative pain assessment records, including VAS at rest at 6 hours and 8 hours after surgery; 7. Complete record of celecoxib use within 24 hours after surgery.

Exclusion criteria

Exclusion criteria: 1. The presence of severe cardiac, pulmonary, liver, kidney dysfunction or other systemic diseases may affect the assessment of analgesic efficacy; 2. History of local anesthetic allergy or contraindications for regional nerve block; 3. Preoperative presence of chronic pain syndromes (such as neuropathic pain, fibromyalgia, etc.) or long-term use of analgesic drugs (> 3 months); 4. During the operation, conversion to general anesthesia, intraspinal anesthesia, or implementation of other regional blocks (such as intercostal nerve block); 5. Missing key information in the electronic medical record (such as postoperative VAS score, celecoxib usage record, block operation description, etc.), and unable to complete the filling in; 6. Preoperative had received other forms of regional nerve block; 7. Postoperative developed severe complications requiring hospitalization.

Design outcomes

Primary

MeasureTime frame
Pain score at rest 8 hours after surgery;

Secondary

MeasureTime frame
Pain score at rest 6 hours after surgery;Usage of Celecoxib;

Countries

China

Contacts

Public ContactChen Xinming

Shenshan Central Hospital, Sun Yat-sen Memorial Hospital, Sun Yat-sen University

chenxm99@mail.sysu.edu.cn+86 151 1942 2666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026