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The effect of continuous use of S(+)-ketamine in the perioperative period on postoperative depression in breast cancer patients: a randomized controlled, double-blind study

The effect of continuous use of S(+)-ketamine in the perioperative period on postoperative depression in breast cancer patients: a randomized controlled, double-blind study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200061575
Enrollment
Unknown
Registered
2022-06-29
Start date
2022-06-15
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Depression

Interventions

ESK group:During the induction of intoxication, S(+)-ketamine 0.5 mg/kg (diluted to 5 ml with normal saline) was given after the patient lost consciousness, and S(+)-ketamine 0.25 mg/kg/h (diluted wit
NS group:During anesthesia induction, 5ml of normal saline was given after the patient's consciousness disappeared, and 0.25ml/kg/h of normal saline was given during the anesthesia maintenance phase.

Sponsors

Ethics Committee of Hangzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who received modified radical mastectomy for unilateral breast cancer; 2. Age 18-65 years old; 3. American Society of Anesthesiologists (ASA) Physical Condition Class I-II; 4. Body mass index (BMI) 18-40 kg/m2; 5. Fully informed consent and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with other mental illnesses such as schizophrenia, mania, or a history of mental illness; 2. Patients who have received psychotropic medication; 3. Uncontrolled high blood pressure, elevated intraocular pressure; 4. Patients with other serious systemic diseases (including severe heart, kidney and liver disease); 5. Allergic to the drugs used in this study.

Design outcomes

Primary

MeasureTime frame
Hamilton-17 Rating Scale (HAMD-17) Score;

Secondary

MeasureTime frame
Venous blood;Serum 5-HT level;Changes of heart rate and blood pressure before and after intubation;Heart rate and blood pressure changes every 5 minutes during anesthesia maintenance;Recovery time;VAS pain score 30min after extubation;VAS pain score 24h after surgery;

Countries

China

Contacts

Public ContactXinlei Lu

Hangzhou First People's Hospital

mazuiluxinlei@163.com+86 17681957300

Outcome results

None listed

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