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Effect of anterior serratus nerve block with bupivacaine liposomal on post-mastectomy pain syndrome

Effect of anterior serratus nerve block with bupivacaine liposomal on post-mastectomy pain syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087643
Enrollment
Unknown
Registered
2024-07-31
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

Anesthesiology

Interventions

Bupivacaine hydrochloride and bupivacaine liposome mixture group:a mixture of bupivacaine hydrochlorideand bupivacaine liposomes
Bupivacaine hydrochloride group:bupivacaine hydrochloride

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-65 years old. 2. ASA I-III. 3. Those scheduled to undergo breast cancer surgery under intubation general anesthesia. 4. Those sent to PACU for resuscitation after surgery.

Exclusion criteria

Exclusion criteria: 1.Patients with difficult airway; 2.Patients with cardiac, hepatic and renal dysfunction; 3.Patients with allergy to study medications; 4.Patients with respiratory tract infection in the last two weeks; 5.Patients withinfection at the point of needle entry; 6.Patients with severe anemia, shock, metabolic disease, electrolyte disorders; 7.Patients with gastric retention or delayed gastric emptying. 8.Communication barriers.

Design outcomes

Primary

MeasureTime frame
Incidence of post-mastectomy pain syndrome;

Secondary

MeasureTime frame
Exercise versus resting VAS pain scores upon leaving the PACU, postoperative (1 day, 2 days, 3 days);Vital signs(blood pressure, HR, SpO2, RR, BIS);Total vasoactive drug use;Total anesthetic drugs;Surgical time, anesthesia time, awakening time;Comfort Evaluation;Preoperative anxiety score;Dosage of analgesics at 1, 2, and 3 days postoperatively;Duration of sensory block in patients;

Countries

China

Contacts

Public ContactXuehai Guan

The First Affiliated Hospital of Guangxi Medical University

guan_xh@aliyun.com+86 185 8769 7310

Outcome results

None listed

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