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Effect of different doses of nalbuphine on ED50 of ciprofol in painless hysteroscopy

Effect of different doses of nalbuphine on ED50 of ciprofol in painless hysteroscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083046
Enrollment
Unknown
Registered
2024-04-15
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

patients who undergoing painless hysteroscopy

Interventions

0.10mg/kg nalbuphine group:patients' somatokinetic response when the hysteroscope enter cervix
0.15mg/kg nalbuphine group:patients' somatokinetic response when the hysteroscope enter cervix
0.20mg/kg nalbuphine group:patients' somatokinetic response when the hysteroscope enter cervix

Sponsors

The First Affiliated Hospital of Shantou University Medical College
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.patients who undergoing elective painless hysteroscopy 2.age 18-65 years old 3.ASA Grade ?-? 4.BMI18-28kg/m2 5.without respiratory diseases and normal airway assessment before surgery

Exclusion criteria

Exclusion criteria: 1.refused to sign the informed consent 2.allergic to the experimental drug 3.complicated with severe circulatory, respiratory, hepatic, urinary, neurological system and mental diseases 4.long-term use of opioids, painkillers, sedatives, or a history of alcohol abuse 5.patients with OSAS 6.with chronic pelvic pain before sugery

Design outcomes

Primary

MeasureTime frame
somatokinetic response;

Secondary

MeasureTime frame
NRS scale;Ramsay Scale;

Countries

China

Contacts

Public ContactZhaodong Zeng

The First Affiliated Hospital of Shantou University Medical College

zzd770@163.com+86 131 1256 8837

Outcome results

None listed

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