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The effect of rimazole alone on postoperative inflammatory response after ureteral stone lithotripsy: a randomized, double-blind, parallel controlled trial

The effect of rimazole alone on postoperative inflammatory response after ureteral stone lithotripsy: a randomized, double-blind, parallel controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070006
Enrollment
Unknown
Registered
2023-03-31
Start date
2023-04-01
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

Ureteral calculus

Interventions

group P:Total intravenous infusion of propofol
group R:Total intravenous pumping of rimazole

Sponsors

Affiliated Hospital of Guangdong Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary participation and the ability to provide informed consent; 2. ASA classification I~III; 3. Patients undergoing selective ureteroscopic holmium laser lithotripsy; 4. Aged 18-75 years, BMI 18-30 kg/m2; 5. Not participated in clinical trials of other drugs in the three months before screening.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to the active ingredients or all excipients of remazolam and benzodiazepines; 2. Patients with schizophrenia and severe depression; 3. Patients taking sedative and hypnotic drugs for a long time; 4. Complicated with other important organ dysfunction: including severe liver and kidney dysfunction; Cerebral organic diseases, specifically aneurysmal vascular diseases or arteriovenous malformations and cerebral hemorrhage; Severe hypertension, coronary heart disease, cardiac insufficiency (NYHA >= grade III), pulmonary hypertension; Hematological diseases; Abnormal coagulation function; Severe respiratory diseases; 5. Patients considered unsuitable for inclusion by other researchers.

Design outcomes

Primary

MeasureTime frame
Procalcitonin (PCT);

Secondary

MeasureTime frame
blood pressure (BP);heart rate (HR);C-reactive protein (CRP);

Countries

China

Contacts

Public ContactXiaoxia Gu

Affiliated Hospital of Guangdong Medical University

343251863@qq.com+86 137 2903 0217

Outcome results

None listed

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