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CompletedNot applicable

Effect of Esketamine on Perioperative Negative Mood in Patients Undergoing Cardiac Valve Surgery

NCT06608030 · Chinese PLA General Hospital

Closed to entry
Status
Not accepting participants
Not applicable
Phase
142
Target enrolment
2
Study sites
Outside the US

What it is testing

Summary

A multicenter, randomized controlled, blinded prospective study to investigate the effects of esketamine on perioperative anxiety and depression in patients undergoing cardiac valve surgery.

Summary as written by the trial’s own sponsor and published on ClinicalTrials.gov API v2. It is the sponsor’s description, reproduced unedited, not an assessment by this site.

What counts as success

Primary outcome measures

  • Perioperative anxiety and depreession

    Measured over Preoperative day 1, postoperative day 7 and day 30

A trial succeeds or fails on its primary outcome, declared in advance. Everything else it reports is secondary by definition.

Who can take part

Eligibility, as published

18 Years
Ages
All
Sex
Not accepted
Healthy volunteers
Inclusion Criteria: 1. Age ≥18 years old, male or female 2. Patients undergoing heart valve surgery 3. Patients with ASA grade 1 to 4 4. BMI between 18-30 kg/m² 5. Able to participate in neuropsychological testing and receive follow-up visits 6. Clearly understand and voluntarily agree to participate in the study and sign the informed consent form Exclusion Criteria: 1. Patients with significant preoperative neuro-psychiatric disease and cognitive impairment 2. Intellectual disability or a MiniMental State Examination (MMSE) score \<24, or a speech disorder that may compromise their ability to undergo preoperative assessments 3. History of psychoactive drug abuse 5\. Preoperative combined severe hepatic insufficiency or renal insufficiency 6. Any contraindications to ketamine or esketamine, such as refractory hypertension or hyperthyroidism

Where

2 study sites

FacilityCityRegionCountry
First Medical center of Chinese PLA General HospitalBeijingBeijing MunicipalityChina
Beijing Tiantan HospitalBeijingBeijing MunicipalityChina

On the registry

Contact the trial directly

This site does not enrol anyone and is not involved in this trial. To ask about taking part, use the sponsor’s own contact details on the official registry record, which is also where the most current version of everything above lives.

Before you do, the preparation checklist lists what a site will ask you on a first call and what is worth asking them. It is free and collects nothing.

NCT06608030 on ClinicalTrials.gov →

Last updated in the registry 2025-11-25. Registry records change; this page reflects the data build of 2026-08-25.

Related

Where this trial sits