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The Median Effective Dose of Ciprofol Combined With Sufentanil for Inhibiting the Gastroscope Insertion in Obese Patients

The Median Effective Dose of Ciprofol Combined With Sufentanil for Inhibiting the Gastroscope Insertion in Obese Patients: a Prospective, Single-center Study

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086298
Enrollment
Unknown
Registered
2024-06-28
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Obese patients who require painless gastroscopy

Interventions

Normal group:Sufentanil (0.1ug/kg) + ciprofol dose determined by modifed Dixon’s up and down method. In the first patient, ciprofol dose was 0.4mg/kg and the dose gradient was 0.01mg/kg. The ‘movement
Obesity group:Sufentanil (0.1ug/kg) + ciprofol dose determined by modifed Dixon’s up and down method. In the first patient, ciprofol dose was 0.4mg/kg and the dose gradient was 0.01mg/kg. The ‘movemen

Sponsors

The First People’s Hospital of Yancheng
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1) Age: 18-64; 2) 18.5=BMI<24.0 kg/m2 or BMI=28 kg/m2 3) ASA grade I-III patients undergoing painless gastroscopy.

Exclusion criteria

Exclusion criteria: 1)Patients who were allergic to sedative/anesthetic drugs such as sufentanil and cyclopofol or had a history of severe allergy; 2) Patients who had contraindications to endoscopy or were refused to anesthesia; 3) Patients without accompanying family members; 4) Uncontrolled severe hypertension (SBP=180mmHg, DBP=110mmHg); 5) Patients with recent acute respiratory infection, acute attack of asthma, acute attack of COPD or preoperative combination of hypoxemia; 6) Acute coronary syndrome, severe arrhythmia, heart rate failure; 7) Massive hemoptysis in active period; 8) Severe anemia (Hb < 6g/dL) 9) Patients with mental system diseases and cognitive dysfunction who cannot communicate normally; 10) Have a history of psychotropic and narcotic drug abuse; 11) Liver dysfunction (Child-Pugh grade C or above); Renal dysfunction (CKD3 stage or above); 12) Pregnant or lactating women; 13) Acute upper gastrointestinal bleeding with shock, pyloric obstruction, achalasia of cardia, gastric emptying disorder, and a history of upper gastrointestinal surgery.

Design outcomes

Primary

MeasureTime frame
The median effective dose of ciprofol;

Secondary

MeasureTime frame
Incidence of perioperative hypotension;Incidence of perioperative bradycardia;Incidence of perioperative hypoxemia;Incidence of postoperative nausea and vomiting;Patient satisfaction;Endoscopist satisfaction;The recovery time of patient;The length of stay in the PACU;

Countries

China

Contacts

Public ContactZhouya Xue

The First People’s Hospital of Yancheng

xuezhouya@163.com+86 157 0511 7696

Outcome results

None listed

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