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Effect of intraoperative esketamine administration on postoperative depression among obese patients undergoing bariatric surgery: a randomized controlled trial.

Effect of intraoperative esketamine administration on postoperative depression among obese patients undergoing bariatric surgery: a randomized controlled trial.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086102
Enrollment
Unknown
Registered
2024-06-25
Start date
2024-07-24
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

depression

Interventions

S group:intraoperative esketamine administration
C group:intraoperative saline administration

Sponsors

HUASHAN HOSPITAL FUDAN UNIVERSITY
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1) at the age of 18 to 60 2) BMI = 30 kg/m^2 3) preoperative PHQ-9 score = 5 4) American College of Anesthesiologists (ASA) Grade II~III 5) Laparoscopic sleeve gastrectomy without contraindications 6) the patient has signed an informed consent form

Exclusion criteria

Exclusion criteria: 1) patients who refuse to participate in clinical trials, refuse to sign informed consent forms or participate in other studies in the same period 2) severe neurological lesions (such as epilepsy) 3) have a history of severe respiratory diseases (such as severe asthma, COPD, respiratory dysfunction, etc.) 4) have a history of severe heart disease (such as severe cardiac insufficiency, malignant arrhythmia, etc.) 5) have a history of severe mental illness (such as schizophrenia, severe depression) or a history of drug abuse 6) people who are allergic to conventional anesthetics or have contraindications (propofol, fentanyl, rocuronium, etc.) 7) there are contraindications for esmolamine drugs, such as intracranial hypertension, unstable angina pectoris, heart failure, myocardial infarction, thoracic or abdominal aortic aneurysms, etc. 8) pregnancy or lactation

Design outcomes

Primary

MeasureTime frame
Patient Health Questionnaire-9 items, PHQ-9;

Secondary

MeasureTime frame
Generalized Anxiety Disorder, GAD-7;incidence of PONV ;

Countries

CHINA

Contacts

Public ContactYingwei Wang; Bairu Liu

HUASHAN HOSPITAL FUDAN UNIVERSITY

1244167738@qq.com+86 152 7482 4480

Outcome results

None listed

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