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To evaluate the effect of ultrasound-guided modified intercostal nerve block in breast cancer surgery

To evaluate the effect of ultrasound-guided modified intercostal nerve block in breast cancer surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300075445
Enrollment
Unknown
Registered
2023-09-05
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-09-11

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:No intervention
High volume group:Modified intercostal nerve block was performed with 40ml 0.33% ropivacaine
Low volume group:Modified intercostal nerve block was performed with 20ml 0.33% ropivacaine

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 undergoing elective breast cancer surgery 2. Aged 18-65 years old 3.ASA ?-? 4. Weight 50-80kg

Exclusion criteria

Exclusion criteria: 1. Contraindications to nerve block, including but not limited to allergy to anesthetics, coagulopathy, and injection site infection (2) opioid use for more than 4 weeks or preoperative chronic pain for more than 3 months 3. Have severe comorbidities, including but not limited to renal insufficiency (creatinine >442moL/L or need for renal replacement therapy), hepatic insufficiency and heart failure, or ASA grade =IV 4.BMI>35kg/m² or <15 kg/m2 5. Accompanied by inability to accurately participate in the evaluation of postoperative analgesia 6. The anatomy of ultrasound scan was difficult, and nerve block surgery could not be performed 7. No informed consent was obtained

Design outcomes

Primary

MeasureTime frame
NRS scores at rest and during activity at 12h after surgery;Remifentanil usage;

Secondary

MeasureTime frame
NRS scores at rest and during activity after postoperative recovery;NRS scores at rest and during activity at 6h after surgery;NRS scores at rest and during activity at 24h after surgery;NRS scores at rest and during activity at 48h after surgery;NRS scores at rest and during activity at 72h after surgery;Intraoperative hemodynamic fluctuations;The incidence of postoperative delirium;Postoperative anxiety and depression;Postoperative sleep quality;

Countries

China

Contacts

Public ContactXu Guanghong

the First Affiliated Hospital of Anhui Medical University, 218 Jixi Road, Hefei, Anhui 230022, China

xuguanghong2004@163.com+86 138 5694 9535

Outcome results

None listed

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