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Esketamine improves postoperative depression in elderly patients with depressed gastrointestinal tumors undergoing laparoscopic surgery

Esketamine improves postoperative depression in elderly patients with depressed gastrointestinal tumors undergoing laparoscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091020
Enrollment
Unknown
Registered
2024-10-18
Start date
2024-04-02
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Gastrointestinal tumors

Interventions

Intervention Group:Intravenous injection of 0.3mg/kg of ketamine during anesthesia induction
Conrol group:Intravenous injection of normal saline during anesthesia induction

Sponsors

Changzhi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1) Elderly patients over 60 years old; (2) Clear consciousness and no abnormal mental state (3) ASA level I-III; (4) Selective surgery; (5) Agree to use postoperative intravenous patient-controlled analgesia. (6) PHQ score>5 points (7) Voluntary signing of informed consent form

Exclusion criteria

Exclusion criteria: (1) Taboos for the use of ketamine (such as grade 3 hypertension, hyperthyroidism, severe heart disease allergies); (2) Sleep apnea syndrome; (3) Intraoperative blood loss = 500ml; (4) Communication barriers; (5) Previously known during surgery; (6) Preoperative concurrent chronic pain; (7) Postoperative admission to the intensive care unit for treatment (8) Patients with a history of dementia or mental illness, or those taking antipsychotic or antidepressant drugs at home

Design outcomes

Primary

MeasureTime frame
depressed;Sleep monitoring;

Secondary

MeasureTime frame
BDNF;5-HT;TNF-a;IL-6;Adverse reactions within 24 hours after surgery;

Countries

China

Contacts

Public ContactJianing Bo

Changzhi People's Hospital

1604719043@qq.com+86 188 3456 2242

Outcome results

None listed

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