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The efficacy and safety of different doses of subanesthetic esketamine combined with propofol in painless gastrological endoscopy

The efficacy and safety of different doses of subanesthetic esketamine combined with propofol in painless gastrological endoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076647
Enrollment
Unknown
Registered
2023-10-13
Start date
2023-10-16
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Painless gastrological endoscopy

Interventions

Propofol group:0.1-0.2ug/kg sufentanil (Renfu Pharmaceutical) and 1-2mg/kg propofol (Sichuan Guorui Pharmaceutical) were given.
Esketamine 1 group:After giving 0.2mg/kg Esketam (jiangsu hengrui Pharmaceutical), 1-2mg/kg propofol (Sichuan Guorui Pharmaceutical) was given.
Esketamine 2 group:After giving 0.3mg/kg Esketam (jiangsu hengrui Pharmaceutical), 1-2mg/kg propofol (Sichuan Guorui Pharmaceutical) was given.
Esketamine 3 group:After giving 0.4mg/kg Esketam (jiangsu hengrui Pharmaceutical), 1-2mg/kg propofol (Sichuan Guorui Pharmaceutical) was given.

Sponsors

Affiliated Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients aged between 18 and 65, regardless of sex, with ASA grade I-II, weighing between 45 and 70 kg, are planned to undergo painless gastrointestinal endoscopy.

Exclusion criteria

Exclusion criteria: Patients with acute upper respiratory tract infection, asthma attack, acute severe throat disease and abnormal liver function; Patients who are allergic to benzodiazepines, fluoroMasini, opioids, propofol, egg products or soybeans; Patients with adrenocortical insufficiency, porphyria or chronic corticosteroid therapy; Patients with airway difficulty and hemodynamic instability (systolic blood pressure [SBP] 180 mmHg, diastolic blood pressure [DBP]>110 mmHg, peripheral blood oxygen saturation [SpO2]<90% under air inhalation); Patients with a history of sleep apnea; Addiction to alcohol, opioids or sedatives and hypnotics.

Design outcomes

Primary

MeasureTime frame
Heart rate;Blood pressure;Pulse oxygen saturation;Anesthesia onset time;Total amount of propofol added;

Secondary

MeasureTime frame
Awakening event;PADSS grade;

Countries

China

Contacts

Public ContactYunqiang Wan

Affiliated Hospital of Southwest Medical University

124559421@qq.com+86 182 0017 3975

Outcome results

None listed

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