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Effect of different ultrasound-guided nerve block schemes on postoperative quality of recovery in patients undergoing mastectomy under general anesthesia

Effect of different ultrasound-guided nerve block schemes on postoperative quality of recovery in patients undergoing mastectomy under general anesthesia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059428
Enrollment
Unknown
Registered
2022-04-29
Start date
2022-07-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Breast cancer

Interventions

Group 1 :Ultrasound-guided paravertebral nerve block before anesthesia induction
Group 2:The serratus anterior muscle block was performed under ultrasound guidance before induction of anesthesia
Group 3:Anterior transverse thoracic combined with serratus anterior plane block before induction of anesthesia

Sponsors

The First Affiliated Hospital of Chengdu Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years; 2. ASA I-II; 3. Mastectomy.

Exclusion criteria

Exclusion criteria: 1. Patients who have contraindications for nerve block (allergy to the anesthetic used in this study, severe coagulation abnormalities, obvious abnormal platelet count, infection at the puncture site, etc.) or who refuse to accept nerve block, and are morbidly obese (BMI > 40 kg/m2) and high-risk patients with malignant hyperthermia; 2. People with a history of mental and neurological diseases, alcohol and drug abuse, and long-term use of opioids or stable drugs; 3. Preoperative radiotherapy and chemotherapy, preoperative chronic pain, preoperative chronic pain, neuromuscular disease, pregnancy; 4. Patients who are unable to cooperate with this study due to certain reasons (such as deafness, blindness, language communication barriers, etc.); 5. Patients lost to follow-up.

Design outcomes

Primary

MeasureTime frame
Numeric Pain Score;15-item Recovery Quality Rating Scale, QoR-15;Additional postoperative analgesic drug dosage;

Secondary

MeasureTime frame
Incidence of postoperative complications;

Countries

China

Contacts

Public ContactShun Wang

The First Affiliated Hospital of Chengdu Medical College

635245417@qq.com+86 18148040132

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 8, 2026