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the clinical study of dexmedetomidine on systemic inflammatory response syndrome(SIRS) and renal damage after percutaneous nephrostolitho tomy (PCNL)

the clinical study of dexmedetomidine on systemic inflammatory response syndrome(SIRS) and renal damage after percutaneous nephrostolitho tomy (PCNL)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15006167
Enrollment
Unknown
Registered
2015-02-13
Start date
2015-02-21
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Systemic inflammatory response syndrome (SIRS)

Interventions

Group D:dexmedetomidine 1ug/kg I.V.

Sponsors

The Third Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Volunteered for the patients, and sign the informed consent; 2. 18-65 year old; 3. Complexity kidney stones (casting, multiple stones and huge stones > 2 cm in diameter); 4. ASA I-II; 5. weight 50~80 kg.

Exclusion criteria

Exclusion criteria: 1. The patient refused to participate in this study; 2. The patients with other important organ dysfunction, including serious liver and kidney dysfunction, NYHA >=III level, coagulant function abnormality; 3. with Sick sinus syndrome, bradycardia (HR <55 times/min), more than ?degree atrioventricular block, tachycardia; 4. History of ipsilateral kidney operation; 5. The history of dexmedetomidine allergy; 6. History of neurological and psychiatric diseases, history of long-term use of sedative drugs, or inappropriate patients for other reasons.

Design outcomes

Primary

MeasureTime frame
heart rate;breathing rate;temperature;WBC;SCr;

Secondary

MeasureTime frame
Inflammatory cytokines;KIM-1;

Countries

China

Contacts

Public ContactShaoli Zhou
shoulizhou@139.com+86 13610272308

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 23, 2026