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The optimal dose of sufentanil during induction of double - lumen bronchial intubation with combined etomidate and esketamine

The optimal dose of sufentanil during induction of double - lumen bronchial intubation with combined etomidate and esketamine

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500104291
Enrollment
Unknown
Registered
2025-06-13
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Lung cancer and lung nodules

Interventions

C Group:Administer 10ml of normal saline
E1 Group:Administer 0.3 mg/kg of esketamine.
E2 Group:Administer 0.5 mg/kg of esketamine.

Sponsors

Hainan Affiliated Hospital of Hainan Medical University(Hainan General Hospital )
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients undergoing thoracoscopic surgery at the People’s Hospital of Hainan Province from January 2025 to December 2026 were selected, with ASA I - II classification, aged 18 - 65 years, and a body mass index (BMI) of 18.5 - 27.9 kg/m^2, who voluntarily participated in the study

Exclusion criteria

Exclusion criteria: Patients with cognitive or language deficits impairing communication and cooperation, psychiatric disorders, intracranial hypertension, or glaucoma were excluded. Those with ischemic heart disease, poorly controlled hypertension (resting SBP >180 mmHg or DBP >100 mmHg), drug/alcohol use, ketamine addiction, difficult airway, reactive airway disease, acute upper respiratory infection, or high aspiration risk were also excluded. Additionally, patients allergic to ketamine or etomidate, with hyperthyroidism, pregnant or breastfeeding women, those in clinical trials within the past 3 months, and those declining study participation were ineligible.

Design outcomes

Primary

MeasureTime frame
Presure;Heart rate;Postoperative delirium;

Secondary

MeasureTime frame
Recovery time;Postoperative nausea and vomiting;

Countries

China

Contacts

Public ContactJiale Li

Hainan Affiliated Hospital of Hainan Medical University(Hainan General Hospital )

kyjiale@qq.com+86 177 8120 9576

Outcome results

None listed

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