Clinical Trials Directory

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UnknownNCT05155969

Intravenous Esketamine on Prevention of Postoperative Depression in Patients Undergoing Cardiac Surgery

Evaluating the Effect of Subanaesthetic Dose of Esketamine on Prevention of Postoperative Depression in Patients Undergoing Cardiac Surgery:a Randomized, Double-blind, Placebo-controlled Pilot and Feasibility Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
80 (estimated)
Sponsor
Anshi Wu · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Esketamine is a general anesthetic with anti-depressant effects at subanaesthetic doses. This study hypothesized that intraoperative administration of ketamine would prevent or mitigate postoperative depressive symptoms in surgical patients.

Detailed description

Single subanaesthetic doses of i.v. esketamine may significantly improve symptoms in psychiatric patients with major depression. In patients undergoing cardiac surgery, postoperative depressive symptoms are common. This study hypothesizes that low-dose esketamine has a preventive effect on postoperative depression. However, evidence in this aspect is insufficient. The purpose of this study is to investigate the effect of a subanaesthetic dose of ketamine on POD for patients undergoing cardiac surgery.

Conditions

Interventions

TypeNameDescription
DRUGEsketamineesketamine (0.3 mg/kg in 100 ml normal saline) is intravenously infused 40 minutes before anesthesia induction
DRUGNormal salineNormal saline will be administrated intravenously at the dural opening, with a total dose of 0.5 ml/kg and continual infusion for 40 minutes.

Timeline

Start date
2021-12-01
Primary completion
2021-12-05
Completion
2022-12-15
First posted
2021-12-14
Last updated
2021-12-14

Locations

2 sites across 1 country: China

Source: ClinicalTrials.gov record NCT05155969. Inclusion in this directory is not an endorsement.