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Median effective dose of prophylactic analgesia with naborphine for the patients' pain during recovery period of gynecological endoscopic surgery

Median effective dose of prophylactic analgesia with naborphine for the patients' pain during recovery period of gynecological endoscopic surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030375
Enrollment
Unknown
Registered
2020-02-29
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Uterine disease

Interventions

Group C:Intravenous saline before induction of anesthesia
Group P (P1, P2, P3, P4, P5):Different doses of nalbuphine before induction

Sponsors

Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >= 45 years; 2. Patients who need laparoscopic hysterectomy; 3. ASA I-II; 4. Patients weighing 50-70kg; 5. Patients who do not use analgesia pump after operation; 6. Patients who sign informed consent and are willing to be followed up.

Exclusion criteria

Exclusion criteria: 1. People who are allergic to naborphine; 2. With history of chronic pain; 3. With history of opioid addiction; 4. Inability to assess pain properly; 5. With application of non-steroidal anti-inflammatory drugs before surgery; 6. There are important organ diseases such as liver and kidney; 7. Have respiratory, circulatory and endocrine system diseases; 8. Patients who are participating in other experiments.

Design outcomes

Primary

MeasureTime frame
NRS score;VAS score at various time points after surgery;

Secondary

MeasureTime frame
Hemodynamic indicators at various time points during the operation;Cough score during extubation;Sedation score 10 minutes after extubation;Incidence of adverse reactions within 24 hours after surgery;

Countries

China

Contacts

Public ContactQi Dunyi

Department of Anesthesiology, Affiliated Hospital of Xuzhou Medical University

qdy6808@163.com+86 15162159886

Outcome results

None listed

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