Clinical Trials Directory

Trials / Completed

CompletedNCT06530706

Effect of Esketamine on Anxiety State in Patients Undergoing Abdominal Tumor Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
185 (actual)
Sponsor
Zhejiang Cancer Hospital · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

To evaluate whether esketamine can relieve anxiety in patients undergoing abdominal tumor surgery.

Detailed description

Hamilton anxiety Scale was used to screen patients with anxiety. Only patients with score ≥ 8 were enrolled. These patients were randomly assigned to the experimental group and control group. All patients enrolled were evaluated with Hamilton anxiety Scale, PHQ-8 scale, QoR-15 Scale and Athens Insomnia Scale. After induction, sevoflurane and remifentanil were used to maintain anesthesia. The experimental group had esketamine while the control group had normal saline. Athens Insomnia Scale was used to assess the sleep status 1, 2, 3 days after surgery and 1 month after surgery. Hamilton anxiety Scale was used to evaluate the anxiety state of the patients 3 days after surgery and 1 month after surgery. PHQ-8 scale, QoR-15 Scale were collected 3 days after surgery and 1 month after surgery.

Conditions

Interventions

TypeNameDescription
DRUGEsketamineEsketamine 0.2mg/kg was pumped slowly after intubation, followed by 0.1mg/kg pumped until the end of the operation. In the PCIA pump, esketamine 1mg/kg was added to the sufentanil.
DRUGnormal salineSame volume of normal saline was pumped slowly after intubation, followed by the same volume of NS until the end of the operation. In the PCIA pump, only sufentanil was used.

Timeline

Start date
2024-08-05
Primary completion
2025-05-30
Completion
2025-06-30
First posted
2024-07-31
Last updated
2025-09-16

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06530706. Inclusion in this directory is not an endorsement.