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Effect of esketamine adjunct to propofol in male patients undergoing rigid cystoscopic ureteral stent removal

Phase 4
Conditions
Urolithiasis
Registration Number
ChiCTR2400088880
Lead Sponsor
The First People's Hospital Of Hangzhou Lin'an District
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

(1)Male patients, aged 18 to 65 years, BMI 18-28 kg/m2<br>(2)ASA physical status I–II<br>(3)scheduled for rigid cystoscopic ureteral stent removal

Exclusion Criteria

(1) abnormal urinary tract anatomy; <br>(2) unstable heart diseases; <br>(3) hyperthyroidism; <br>(4) central nervous system diseases; <br>(5) neuropsychiatric disorders or drug abuse; <br>(6) allergic to the study drugs; <br>(7) ocular hypertension.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of intraoperative hypoxemia;
Secondary Outcome Measures
NameTimeMethod
total propofol dosage;Incidence of adverse events;
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