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Effect of Esketamine on analgesic and anti-depression in patients after laparoscopic resection of gastric carcinoma

Effect of Esketamine on analgesic and anti-depression in patients after laparoscopic resection of gastric carcinoma

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072167
Enrollment
Unknown
Registered
2023-06-05
Start date
2023-01-18
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Gastric cancer

Interventions

Control group:Normal saline was used for control during perioperative period
Esketamine group:Esketamine was used perioperatively

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: (1) American Society of Anesthesiologists (ASA) medical condition I~II, no respiratory or circulatory disorders, no chronic pain, definite diagnosis of gastric cancer (refer to the diagnostic criteria of Health Industry of the People's Republic of China: Diagnostic Criteria for Gastric Cancer (WS 316-2010)). (2) Patients who were willing to receive PCIA after elective laparoscopic surgery for gastric cancer. (3) The age range is over 18 years old. (4) Able to understand the procedures and methods of this study and willing to sign the informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria: (1) History of radiotherapy and chemotherapy for gastric cancer. (2) Have mental disorders, mental disorders and other diseases. (3) A history of depression. (4) Severe hypertension, coronary heart disease, cardiac insufficiency, pulmonary hypertension, cranial or ocular hypertension, hyperthyroidism, etc. (5) Patients with allergic history of the drugs used in this study. (6) Emergency surgery or trauma patients. (7) It is expected that the operation time will be long, there is the possibility of large amount of blood loss, or there is laparotomy transfer during the operation.

Design outcomes

Primary

MeasureTime frame
postoperative pain;

Secondary

MeasureTime frame
Postoperative depression;Postoperative anxiety;Postoperative fatigue;PT;APTT;

Countries

China

Contacts

Public ContactGeng Wujun

The First Affiliated Hospital of Wenzhou Medical University

gengwujunok@163.com+86 135 8743 0257

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026