Skip to content

The effect of Esketamine in gynecological laparoscopic radical resection of malignant tumor on patients' rapid recovery

The effect of Esketamine in gynecological laparoscopic radical resection of malignant tumor on patients' rapid recovery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084149
Enrollment
Unknown
Registered
2024-05-11
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Gynecological malignant tumor

Interventions

K group:Esketamine 0.5mg/kg was injected intravenously before skin incision.
C group:Inject the same dose of saline before skin incision.

Sponsors

Xing' an league people's hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-65 years; (2) It is planned to perform elective gynecological laparoscopic radical resection of malignant tumor under general anesthesia; (3) The 3)ASA score is ? ~ ?; (4) The estimated survival time is more than 3 months; (5) Voluntary signing of informed consent.

Exclusion criteria

Exclusion criteria: (1) patients who are expected to enter ICU after operation; (2) Patients who are allergic to Esketamine Injection; (3) Patients with mental system diseases, severe consciousness disorders and cognitive dysfunction; (4) Have a serious cardiovascular history: congestive heart failure, severe angina pectoris, unstable angina pectoris or myocardial infarction within 6 months; (5) Pregnant or lactating patients; (6) Patients with 6)MMSE score < 18; (7) Patients with any of the following contraindications to the use of Esketamine Injection: (1) Patients with severe blood pressure or increased intracranial pressure risk; 2) Patients with high intraocular pressure (glaucoma) or penetrating ocular trauma; 3) poorly controlled or untreated hypertension (resting systolic blood pressure exceeds 180mmHg or diastolic blood pressure exceeds 100 mmHg); 4) Patients with hyperthyroidism; 5) Preeclampsia and eclampsia; 6) Use it when a uterine relaxant is needed.

Design outcomes

Primary

MeasureTime frame
NRS pain score was evaluated within 48 hours after operation.;

Secondary

MeasureTime frame
Time of laryngeal mask removal;Get out of bed activity time;First exhaust time;

Countries

People's Republic of China

Contacts

Public ContactRenjie

Xing' an league people's hospital

627508994@qq.com+86 139 4748 2965

Outcome results

None listed

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