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Study protocol on the effect of low-dose dexamethasone combined with ulinastatin in preventing systemic inflammatory response after intracavitary holmium laser lithotripsy

Study protocol on the effect of low-dose dexamethasone combined with ulinastatin in preventing systemic inflammatory response after intracavitary holmium laser lithotripsy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103934
Enrollment
Unknown
Registered
2025-06-09
Start date
2025-06-09
Completion date
Unknown
Last updated
2025-06-16

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

Conditions

Systemic inflammatory response

Interventions

Dexamethasone group:Administer 10mg of dexamethasone via intravenous drip
Utesitide group:The Utesitide group received 50,000 IU/h of Utesitide through infusion
Combined medication group:Simultaneously administer 10mg of dexamethasone via intravenous drip and 50,000 IU/h of ulinastatin through infusion pump

Sponsors

Leshan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-75 years old, gender is not limited; 2. Diagnosed with upper urinary tract stones, and in line with the surgical indications for endoluminal holmium laser lithotripsy; 3. No systemic infection or severe inflammatory reaction (such as fever, significant increase in white blood cell count, etc.) before surgery; 4. No serious heart, liver and kidney insufficiency; 5. Voluntarily sign the informed consent form and be able to cooperate with the postoperative follow-up.

Exclusion criteria

Exclusion criteria: 1. Systemic infection or active inflammation (such as fever, significantly elevated white blood cell count) before surgery; 2. Known hypersensitivity to dexamethasone, ulinastatin or their components; 3. Recent (within 3 months) use of glucocorticoids or immunosuppressants; 4. Combined with malignant tumors, immune system diseases or hematologic diseases; 5. Pregnant or lactating females; 6. Those who are unable to cooperate with treatment or follow-up.

Design outcomes

Primary

MeasureTime frame
white blood cell;Calcitonin;C-reactive protein;Interleukin-6;

Countries

China

Contacts

Public ContactZhang Mingmin

Leshan People's Hospital

120163347@qq.com+86 139 9068 1138

Outcome results

None listed

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