Skip to content

Effect of Press Needle Combined with Lidocaine-Opioid-Sparing Anesthesia on Remifentanil Consumption and Postoperative Pain Management in Patients Undergoing Breast Cancer Surgery

Effect of Press Needle Combined with Lidocaine-Opioid-Sparing Anesthesia on Remifentanil Consumption and Postoperative Pain Management in Patients Undergoing Breast Cancer Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500108711
Enrollment
Unknown
Registered
2025-09-03
Start date
2025-09-15
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Breast cancer

Interventions

C Group:Sham press needles were implemented 30 minutes before anesthesia induction, and an equivalent volume of normal saline was initiated before anesthesia induction and continuously infused intraop
L Group:Sham press needles were applied 30 minutes before anesthesia induction. While 1% lidocaine (1.5 mg/kg) was intravenously infused over 10 minutes starting 10 minutes before anesthesia induction
NL Group:Press-needle therapy was administered 30 minutes before anesthesia induction, and 1% lidocaine (1.5 mg/kg) was intravenously infused over 10 minutes starting 10 minutes before anesthesia indu

Sponsors

Jiangsu Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: (1) Patients scheduled for unilateral radical mastectomy with ipsilateral sentinel lymph node biopsy (SLNB) or modified radical mastectomy for breast cancer; (2) ASA physical status classification I-II; (3) Age 18-64 years; (4) BMI 18.5-27.9 kg/m²; (5) Patient or family member has provided signed informed consent.

Exclusion criteria

Exclusion criteria: (1) History of allergy to Lidocaine, Opioids, Alcohol, or Adhesive tape; (2) History of analgesic medication use within the past month; (3) Preoperative history of chronic pain in the surgical area; (4) Preoperative severe systemic diseases (e.g., cardiac, pulmonary, hepatic, renal); (5) Received acupuncture or electroacupuncture therapy within the past two weeks; (6) Infection at acupoint sites.

Design outcomes

Primary

MeasureTime frame
Total remifentanil dosage ;Postoperative NRS scores;Postoperative adverse reactions;

Secondary

MeasureTime frame
15-item Recovery Quality Scale;Neutrophil count;Lymphocyte count;The ratio of neutrophils to lymphocytes;Platelet-to-lymphocyte ratio;Vascular endothelial growth factor-A;Matrix metalloproteinase;Interleukin-6;Interleukin-10;Interleukin-17;The incidence of chronic pain 3 months after the operation;

Countries

China

Contacts

Public ContactQingming Bian

The Affiliated Cancer Hospital of Nanjing Medical University & Jiangsu Cancer Hospital & Jiangsu Institute of Cancer Research

bqm2518@njmu.edu.cn+86 25 8328 4765

Outcome results

None listed

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