Skip to content

Study on the effectiveness and safety of opioid free anesthesia for transurethral holmium laser ureteral lithotripsy

Study on the effectiveness and safety of opioid free anesthesia for transurethral holmium laser ureteral lithotripsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099851
Enrollment
Unknown
Registered
2025-03-31
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Holmium laser lithotripsy for ureteral stones

Interventions

Test group:Anesthesia induction drugs: Within 10 minutes, administer a loading dose of 1 µ g/kg of dexmedetomidine by pump, and start anesthesia induction. Administer midazolam 0.03mg/kg, ketamine 0.5
Control group:Anesthesia inducing drugs: midazolam 0.03mg/kg, sufentanil 0.2-0.3 µ g/kg, rocuronium bromide 0.6mg/kg, propofol 2.0mg/kg.Continuous intravenous infusion of remifentanil 0.05-0.20 µ g/kg

Sponsors

Tianjin Fourth Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Participants who fully understood the purpose and significance of this trial, voluntarily agreed to participate, and signed the informed consent form. 2. Hospitalized patients diagnosed with ureteral stones scheduled for holmium laser ureterolithotripsy under general anesthesia with endotracheal intubation. 3. Age >=18 years, regardless of gender. 4. ASA physical status classification I-III.

Exclusion criteria

Exclusion criteria: 1. Refusal to sign informed consent; 2. Diagnosed psychiatric disorders with preoperative communication impairment due to cognitive or language barriers; 3. Uncontrolled or poorly controlled hypertension; 4. Significant risk of elevated blood pressure or intracranial hypertension; 5. Elevated intraocular pressure (glaucoma) or penetrating ocular trauma; 6. Untreated or inadequately treated hyperthyroidism; 7. Sick sinus syndrome with heart rate <50 beats per minute; 8. Severe cardiopulmonary, hepatic or renal comorbidities; 9. History of chronic pain with long-term or recent opioid abuse; 10. Pregnancy or lactation; 11. Known hypersensitivity to trial medications; 12. Participation in other drug trials or medical device studies within preceding 3 months;

Design outcomes

Primary

MeasureTime frame
Postoperative recovery quality;

Secondary

MeasureTime frame
Postoperative nausea and vomiting rate;Postoperative pain score;blood sugar;

Countries

China

Contacts

Public ContactChunjing Zhou

Tianjin Fourth Central Hospital

674033808@qq.com+86 22 2624 9235

Outcome results

None listed

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