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Clinical studies of nalbuphine combined with etomidate in painless gastrointestinal endoscopy

Clinical studies of nalbuphine combined with etomidate in painless gastrointestinal endoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072426
Enrollment
Unknown
Registered
2023-06-13
Start date
2018-04-24
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Patients receiving painless gastroenteroscopy

Interventions

Group C (First part):0.08 mg/kg nalbuphine + 0.2-0.3 mg/kg etomidate
Group D (First part):0.1 mg/kg nalbuphine + 0.2-0.3 mg/kg etomidate
Group A (First part):0.04 mg/kg nalbuphine + 0.2-0.3 mg/kg etomidate
Group B (First part):0.06 mg/kg nalbuphine + 0.2-0.3 mg/kg etomidate
Group P (second part):Palonosetron 0.075 mg iv
Group S (second part):0.1 mg scopolamine hydrobromide iv
Group PS (second part):0.075 mg palonosetron +0.1 mg scopolamine hydrobromide iv
Group C (second part):same volume of saline iv

Sponsors

the 900th Hospital of the Joint Logistics Support Force
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 18-65 for painless gastroscopy, regardless of gender; 2. Body mass index (BMI) 18.5-30 kg/m2; 3. American Society of Anesthesiologists (ASA) I~II.

Exclusion criteria

Exclusion criteria: 1. Cannot meet any inclusion criteria; 2. Refusal to accept anesthesia or sedation; 3. Patients with a history of metabolic diseases such as serious abnormalities of heart, brain, lung, liver, kidney and cortex; 4. Those who have received gastrointestinal surgery or other abdominal surgery; 5. Patients with a history of recovery from abnormal surgical anesthesia; 6. ECG suggested: heart rate 180 mmHg and/or diastolic blood pressure > 110 mmHg in patients with hypertension or < 90/60 mmHg in patients with hypotension before examination; 9. With neuromuscular diseases or mental diseases; 10. Hemoglobin lower than 90 g/L; 11. Suspected abuse of narcotic analgesics or sedatives; 12. Predicting the possibility or history of difficult airway; 13. People who are known to be allergic to emulsions and opioids; 14. Subjects are deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Myoclonic grade;Incidence of nausea and vomiting;

Secondary

MeasureTime frame
Choking cough response;Body dynamic response;Whether additional propofol is needed;behavioral pain scale score for non-intubated, BPS-NI;The length of the examination;The length of time between the end of the examination and the awakening;The length of time from waking up to leaving the operating room;Amount of etomidine;Amount of propofol;blood pressure;Incidence of SpO2 30%;cases of jaw lifting;cases of mask ventilation;Adverse events after awakening;Incidence and intensity of nausea and vomiting;Use of anti-nausea and vomiting drugs;Patient's satisfaction;Duration of dizziness;Duration of drowsiness;Incidence of dry mouth;Incidence of blurred vision;Incidence of headache;

Countries

China

Contacts

Public ContactJianghuai Lin

the 900th Hospital of the Joint Logistics Support Force of the People's Liberation Army

curry26283599@163.com+86 130 5552 4595

Outcome results

None listed

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