Clinical Trials Directory

Trials / Completed

CompletedNCT04850937

Effect of Low-dose Esketamine on Postoperative Depression in Patients With Breast Cancer

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Yangzhou University · Academic / Other
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

esketamine is an optical isomer of ketamine. Compared with ketamine, esketamine has the characteristics of higher effective value, stronger receptor affinity, less adverse reactions of nervous system, and pharmacokinetics is controllable. Domestic and foreign studies have focused on the therapeutic effect of esketamine on major depression, but less attention has been paid to perioperative depression.This study intends to explore the effect of small doses of esketamine on patients with breast cancer.Postoperative depression and pain are observed.

Detailed description

This study intends to explore the effect of small doses of esketamine on patients with breast cancer.WE pay attention to : 1. Safety of low-dose single intravenous injection of esketamine (1)The influence of intraoperative vital signs of patients after medication, such as blood pressure and heart rate fluctuation; (2)the duration of recovery after anesthesia; (3)postoperative adverse reactions, such as nausea and vomiting, dizziness and diplopia, respiratory depression, laryngeal spasm, delirium agitation, etc 2. Effect of single intravenous injection of low-dose ketamine on postoperative depression in patients undergoing radical mastectomy (1) 1 day before surgery, 2 days, 5 days, 30 days, 90 days after surgery Hamilton Depression Scale scores; (2) The serum leptin level 1 day before surgery, 2 days after surgery and 5 days after surgery; (3) Correlation between depression scale score and leptin level 3. Effects of low dose esketamine on acute and chronic pain in patients undergoing radical mastectomy * visual analogue scale scores at 6, 12 and 24 hours after surgery; * visual analogue scale scores at 3, 5, 30 and 90 days after surgery; * the number of analgesic remedies

Conditions

Interventions

TypeNameDescription
DRUGEsketamineThe experimental group will be given 0.25mg/kg esketamine slowly intravenously after anesthesia induction
DRUGnormal salineThe experimental group will be given 0.5ml/kg normal saline intravenously after anesthesia induction

Timeline

Start date
2021-02-10
Primary completion
2021-04-10
Completion
2022-05-10
First posted
2021-04-20
Last updated
2022-07-28

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT04850937. Inclusion in this directory is not an endorsement.