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The impact of postoperative analgesia with butorphanol combined with dexmedetomidine on the quality of life in breast cancer patients

Research protocol on the effect of postoperative analgesia of butorphanol combined with dexmedetomidine on the quality of life of breast cancer patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097689
Enrollment
Unknown
Registered
2025-02-24
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-10-27

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:Postoperatively, sufentanil 0.75ug/kg + dexmedetomidine 0.05ug/kg/h + tropisetron 10mg plus normal saline to 100ml were used for analgesic management, and the drug was administered throu
Experimental group:After the operation, butorphanol 0.15mg/kg + dexmedetomidine 0.05ug/kg/h + tropisetron 10mg plus normal saline to 100ml were used for administration through an intravenous self-cont

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
19 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age > 18 years; 2.The participant voluntarily joins the study and signs the informed consent form; 3.Patients with breast cancer confirmed by pathology are scheduled to undergo radical mastectomy or modified radical mastectomy; 4.American Society of Anesthesiologists (ASA) physical status classification of Grade I-II.

Exclusion criteria

Exclusion criteria: 1.Severe preoperative cardiac, pulmonary, hepatic, or renal insufficiency; 2.History of psychiatric disorders or long-term use of antiepileptic drugs, antidepressants, sedative-hypnotics, or other psychotropic medications; 3.Known allergy to sufentanil, butorphanol, dexmedetomidine, tropisetron, or related agents; 4.BMI 30 kg/m^2; 5.Long-term opioid therapy for chronic pain before surgery; 6.Severe preoperative sinus bradycardia (heart rate < 50 bpm), sick sinus syndrome, second-degree or higher atrioventricular block, or presence of a pacemaker; 7.Pregnancy or lactation; 8.Recent major life events that could affect quality of life; 9.Advanced breast cancer with widespread metastasis; 10.Concomitant malignancy present preoperatively; 11.Preoperative intellectual disability or cognitive impairment preventing effective communication; 12.Any other condition that, in the investigator’s judgment, makes the patient unsuitable for the study.

Design outcomes

Primary

MeasureTime frame
Postoperative quality of life;

Secondary

MeasureTime frame
Pain level;Sleep quality;Anxiety/depressive state;Postoperative adverse reactions;Postoperative fatigue;Use of postoperative analgesics;Patient satisfaction;

Countries

China

Contacts

Public ContactYang xinping

Shenzhen Second People's Hospital

185407707@qq.com+86 158 8958 8400

Outcome results

None listed

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