Skip to content

Prospective study of efficacy of PCNL under local anesthesia based on Enhanced Recovery after Surgery

A single-center, randomized, double-blind, parallel controlled clinical study of the efficacy of percutaneous nephrolithotomy under local and general anesthesia based on Enhanced Recovery after Surgery

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045681
Enrollment
Unknown
Registered
2021-04-23
Start date
2019-06-15
Completion date
Unknown
Last updated
2021-12-06

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

Conditions

kidney stone

Interventions

Group 1:PCNL under ERAS local anesthesia
Group 2:PCNL under ERAS general anesthesia

Sponsors

Gannan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 80 years; 2. Caliceal calculi and single pelvis calculi 1.5 cm; 4. Mild or greater water accumulation; 5. Preoperative approval by the ethics committee of the hospital and informed consent of the family members.

Exclusion criteria

Exclusion criteria: 1. Complex calculi with an estimated time of more than 2 hours; 2. Patients with combined liver and kidney dysfunction, hematopoietic system, cardiovascular and cerebrovascular diseases, kidney and liver and other primary diseases, with ASA score greater than 3 points; 3. Inoperative inability to coordinate the position, including: spinal deformity, poor lung function, etc.; 4. Patients self-assessed poor pain tolerance.

Design outcomes

Primary

MeasureTime frame
Intraoperative and postoperative pain;

Countries

China

Contacts

Public ContactLIU Zhaorong

Gannan Medical University

970179875@qq.com+86 18870443590

Outcome results

None listed

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