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Effects of different doses of esketamine pretreatment on postoperative sore throat after double-lumen endobronchial intubation:A randomized double-blind controlled study

Effects of different doses of esketamine pretreatment on postoperative sore throat after double-lumen endobronchial intubation:A randomized double-blind controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500110242
Enrollment
Unknown
Registered
2025-10-11
Start date
2024-03-08
Completion date
Unknown
Last updated
2025-10-13

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

Conditions

None listed

Interventions

Test group 1:esketamine 0.05mg/kg
Test group 2:esketamine 0.075mg/kg
Test group 3:esketamine 0.1mg/kg
control group:Normal saline 2ml

Sponsors

Lishui People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18 to 65 years old ; 2. Women and men are not limited ; 3. Body Mass Index 20 ~ 30kg / m^2 ; 4. American Society of Anesthesiologists ( ASA ) grade I ~ II ; 5.Patients undergoing elective thoracoscopic lung surgery.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to anesthetics ; 2. Patients with chronic cough, pharyngitis, sore throat, asthma ; 3. Intubation or extubation is not smooth ; 4. Perioperative need through the mouth or through the nose into the stomach tube, nutrition tube ; 5. Severe hypertension, cerebrovascular disease, epilepsy, mental illness, severe organ dysfunction, lactating women, etc. ; 6. Unclear speech can not be evaluated normally.

Design outcomes

Primary

MeasureTime frame
the incidence and severity of sore throat;

Secondary

MeasureTime frame
heart rate;blood pressure;pulse oxygen saturation;dizziness;nausea and vomiting;mental symptom;recovery time;extubation time;bispectral index of EEG;

Countries

China

Contacts

Public ContactDong Xiaoli

Lishui People's Hospital

xuqiaomin810@163.com+86 189 5709 3880

Outcome results

None listed

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