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Clinical observation of postoperative analgesia in patients with breast cancer without an opioid regimen: a single-center randomized controlled study

Clinical observation of postoperative analgesia in patients with breast cancer without an opioid regimen: a single-center randomized controlled study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096199
Enrollment
Unknown
Registered
2025-01-20
Start date
2024-05-10
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

mammary cancer

Interventions

Sufentanil group:Sufentanil 2 ug / kg + halobiprofen ester 100mg + palonosetron 0.25mg=100ml
Esketamine group:Eesketamine 2.5mg / kg + flurbiprofen ester 100mg + palonosetron 0.25mg=100ml
Esketamine and dexmedetomidine group:Eesketamine 2.5mg / kg + dexmedetomidine 2 ug / kg + hallobiprofen ester 100mg + paronosetron 0.25mg=100ml

Sponsors

Hainan Affiliated Hospital of Hainan Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1)> 18 years; (2) American Society of Anesthesiologists (American Society of Anesthesiologists, ASA) grade I-II; (3) not pregnant; (4) diagnosis of breast cancer and proposed radical breast cancer.

Exclusion criteria

Exclusion criteria: (1) body mass index (body mass index, BMI)>30 kg/m²; (2) History of angina pectoris or myocardial infarction in the past 6 months; (3) Unwell-controlled or untreated hypertension (resting systolic / diastolic blood pressure> 180 / 100 mmHg); (4) Untreated or undertreated hyperthyroidism; (5) Liver and renal insufficiency; (6) Neuropsychiatric diseases; (7) Long-term alcoholism; (8) Long-term use of sedative, hypnotic, analgesic and antipsychotic drugs; (9) Heart rate (heart rate, HR) <50 times / min or with III degree atrioventricular block; (10) Know to be allergic to test drugs such as dexmedetomidine and (or) esketamine; (11) Change of the operation mode during the operation; (12) Loss of perioperative

Design outcomes

Primary

MeasureTime frame
anxiety-depression;

Secondary

MeasureTime frame
selep quality ;pain;calm;

Countries

China

Contacts

Public ContactDuozhi Wu

Hainan Affiliated Hospital of Hainan Medical University

13976674619@163.com+86 139 7667 4619

Outcome results

None listed

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