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Effect of different doses of nalbuphine on the effective dose of propofol in suppressing the response to gastroscopy in obese adults

Effect of different doses of nalbuphine on the effective dose of propofol in suppressing the response to gastroscopy in obese adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093032
Enrollment
Unknown
Registered
2024-11-27
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Gastric ulcer, stomach pain and other diseases requiring gastroscopy

Interventions

Nalbuphine group N2:Nalbuphine 0.3mg/kg
Nalbuphine group N1:Nalbuphine 0.15mg/kg

Sponsors

Affiliated Qingyuan Hospital, Guangzhou Medical University,Qingyuan People's Hospital;
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 18 to 65 years undergoing gastroscopy with general anesthesia; 2.ASA grade I-II; 3.BMI more than 28 kg/m2; 4.Able to sign the informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with known history of anaphylaxis to the study plan medication; 2.Irregular control or history of severe hypertension; 3.Severe coronary artery disease, psychosis, chronic pain, pregnancy or planned pregnancy within 3 months, seizures, increased intracranial pressure; 4.Recent (within 3 days) history of use of analgesics, history of drug abuse or use of central nervous system drugs within 6 months; 5.Patients with significant respiratory depression, acute or severe asthma; 6.Known or suspected gastrointestinal obstruction (including paralytic ileus) ;

Design outcomes

Primary

MeasureTime frame
ED50 of propofol;

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;SPO2;Total time of endoscopy,;Time to resuscitation;Length of stay in resuscitation room;Satisfaction of patient;Satisfaction of endoscopist;Incidence of sedation-related adverse events;The first time of use vasoactive drugs;The first time need for airway intervention;

Countries

China

Contacts

Public ContactHuang Yizhou

Affiliated Qingyuan Hospital, Guangzhou Medical University,Qingyuan People's Hospital;

m15715213820@163.com+86 15715213820

Outcome results

None listed

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