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Effect of Esketamine Hydrochloride on Haemodynamic Changes after Tracheal Intubation without Muscle Relaxants: A Randomized Controlled Trial

Effect of Esketamine Hydrochloride on Haemodynamic Changes after Tracheal Intubation without Muscle Relaxants: A Randomized Controlled Trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052973
Enrollment
Unknown
Registered
2021-11-06
Start date
2021-11-08
Completion date
Unknown
Last updated
2022-08-30

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

Conditions

None listed

Interventions

esketamine group:esketamine combined with remifentanil
propofol group:propofol combined with remifentanil

Sponsors

Zhongshan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Thyroidectomy patients receiving neuroelectrophysiological monitoring; 2. Aged 20-60 years; 3. ASA classification I-II; 4. Body mass index (BMI): 18-30 kg/m^2; 5. The patients were tested voluntarily and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Severe cardiovascular disease (NYHA III-IV) or severe arrhythmia; 2. Patients with impaired liver function and/or renal function (ALT and/or AST exceed 2 times the upper limit of normal, BUN and/or SCr exceed 1.5 times the upper limit of normal; 3. Those with a history of asthma or airway hyperresponsiveness; 4. Those who have used sedatives or anesthetics within 24 hours; 5. Patients with mental disorders or mental illnesses; 6. Patients predicted to be difficult airway; 7. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Systolic blood pressure;Diastolic blood pressure;mean arterial blood pressure;Heart rate;

Secondary

MeasureTime frame
Tracheal intubation conditions;RASS score in PACU;

Countries

China

Contacts

Public ContactDu Fang

Zhongshan Hospital, Fudan University

du.fang@zs-hospital.sh.cn+86 13917569701

Outcome results

None listed

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