Overview

Esketamine Combined With Remimazolam on Postoperative Sleep Disturbance and Anxiety in Patients

Status:
Recruiting
Trial end date:
2024-06-10
Target enrollment:
0
Participant gender:
All
Summary
To explore the effects of esketamine combined with remimazolam on postoperative sleep disturbance and anxiety in surgical patients undergoing gastroenteroscopies
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tianjin Medical University General Hospital
Treatments:
Esketamine
Propofol
Criteria
Inclusion Criteria:

1. Age 20-65 years old;

2. ASA classification is grade I-III;

3. Elective surgery is proposed

4. BMI of 19-30 kg/m2;

5. Patients who agreed to enroll in this study voluntarily

Exclusion Criteria:

1. Those who are known to be allergic to the drug ingredients in this study and their
allergic constitution;

2. Allergic history of general anesthesia drugs, opioid drugs, non-steroidal drugs;

3. History of neurological diseases; History of chronic pain; Drug and alcohol addiction;
A long history of opioid use; Opiates were given 48 hours before surgery;

4. ASA rating of IV or V;

5. Coronary heart disease, bronchial asthma, severe hypertension, severe blood system
dysfunction, liver and kidney function, electrolyte abnormalities;

6. History of gastrointestinal disease (peptic ulcer, Crohn's disease, ulcerative
colitis);

7. Respiratory insufficiency, respiratory failure;

8. Patients who refused to use intravenous PCA for analgesia;

9. Pregnant or lactating women;

10. BMI<18 kg/m2 or BMI>30kg/m2;

11. Poor compliance, unable to complete the experiment according to the study plan;

12. Participants who have participated in clinical trials of other drugs within the last 4
weeks;

13. Any circumstances deemed unsuitable for inclusion by the researcher for any reason.