Skip to content

Clinical study for nalbuphine combined with dexmedetomidine as local anesthetic adjuvant in local wound infiltration analgesia after breast cancer surgery

Clinical study for nalbuphine combined with dexmedetomidine as local anesthetic adjuvant in local wound infiltration analgesia after breast cancer surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800018508
Enrollment
Unknown
Registered
2018-09-21
Start date
2018-09-30
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

Breast cancer

Interventions

Group C:0.375% ropivacaine 20ml
Group N: Nalbuphine 10mg+0.375% ropivacaine(20ml)
Group D :Dexmedetomidine 1µg /kg+ 0.375% ropivacaine(20ml)
Group ND:Dexmedetomidine 1µg /kg+ Nalbuphine 10mg+0.375% ropivacaine(20ml)

Sponsors

Department of Anesthesiology, First Affiliated Hospital of Henan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 60 Years

Inclusion criteria

Inclusion criteria: Females of American society of anesthesiologists (ASA) physical status I-II, BMI 18~24kg/m2, aged 35 to 65 years, who were scheduled for radical mastectomy will be included in this study.

Exclusion criteria

Exclusion criteria: History of breast surgery, incision site infection, coagulation dysfunction, drug allergy to local anesthesia, long-term history of opioids or antiemetic drugs, pregnant women, patients with central neuropathy, patients with liver and kidney dysfunction, patients with mental disorders, overweight patients (BMI > 30 kg / m2), patients with hypotension, and patients refusing to participate Add.

Design outcomes

Primary

MeasureTime frame
Nume ricrating scale(NRS) pain score;

Secondary

MeasureTime frame
Ramsay score;blood pressure;heart rate;

Countries

China

Contacts

Public ContactZHENG Xiao-zhen

The First Affiliated Hospital of Henan University

573870613@qq.com+86 13938632449

Outcome results

None listed

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