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To observe the clinical effect of ultrasound-guided modified intercostal nerve block and erector spinal muscle block in breast cancer radical operation

To observe the clinical effect of ultrasound-guided modified intercostal nerve block and erector spinal muscle block in breast cancer radical operation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077956
Enrollment
Unknown
Registered
2023-11-24
Start date
2023-09-01
Completion date
Unknown
Last updated
2023-11-27

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

Conditions

Breast Cancer

Interventions

Control group:erector spinal muscle block
Experimental group:modified intercostal nerve block

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients underwent modified radical mastectomy in our hospital; 2.aged 18 to 65 years old; 3.ASA I-III; 4.weight 40-80kg.

Exclusion criteria

Exclusion criteria: 1.Patients with contraindications to regional block technique(allergy to local anesthetic, infection around puncture site and coagulation disorder); Patients with peripheral neuropathy or sensory abnormalities in the nerve innervated skin area at the puncture site/site that needs to be blocked; 2.Preoperative use of opioid drugs; 3.Patients with heart failure, severe arrhythmia, and severe liver and kidney disease; 4.BMI>35kg/m2; 5.patients with not accurate in evaluating dysfunction postoperative analgesia; 6.Mental Disorders (depression, mania, schizophrenia, or a history of antipsychotic use); 7.Failure to sign an informed consent.

Design outcomes

Primary

MeasureTime frame
pain scores of rest and movement at 6h;

Secondary

MeasureTime frame
Dosage of intraoperative anesthetics,vasoactive drugs and infusion amount;Postoperative hospital stay;Hemodynamics;Postoperative adverse reactions;operation time?anesthesia time;pain scores of rest and movement at 0h,3h,12h,24h after Postoperative awake2;Postoperative Quality of Recovery Score in 24h;The amount of remedial drugs used after surgery;

Countries

China

Contacts

Public ContactGuanghong Xu

The First Affiliated Hospital of Anhui Medical University

xuguanghong2004@163.com+86 138 5694 9535

Outcome results

None listed

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