Evaluation of Two Different Treatments for Lower Pore Renal Stone: Microperc Vs FURS

NCT03307096 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2024-07-09

No results posted yet for this study

Summary

This is a prospect, randomized control trial to evaluate merits between microperc and FURS for lower pole renal stone

Conditions

  • Surgery--Complications
  • Renal Calculus
  • Nephrolithiasis
  • Urolithiasis

Interventions

PROCEDURE

Microperc surgery

Parents are treated by Microperc Percutaneous Nephrolithotomy

PROCEDURE

FURS

Parents are treated by FURS

Sponsors & Collaborators

  • Beijing Friendship Hospital

    collaborator OTHER
  • Renmin Hospital of Wuhan University

    collaborator OTHER
  • Affiliated Hospital of Hebei University

    collaborator OTHER
  • Jiangsu Province Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • West China Hospital

    collaborator OTHER
  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    collaborator OTHER
  • People's Hospital of Anshun City of Guizhou Province

    collaborator OTHER
  • Zhejiang Provincial People's Hospital

    collaborator OTHER
  • The First Affiliated Hospital with Nanjing Medical University

    collaborator OTHER
  • First Affiliated Hospital of Xinjiang Medical University

    collaborator OTHER
  • General Hospital of Shenyang Military Region

    collaborator OTHER
  • Ningbo No. 1 Hospital

    lead OTHER

Principal Investigators

  • Yue Cheng, Dr. · Ningbo No. 1 Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-11-17
Primary Completion
2019-10-01
Completion
2019-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03307096 on ClinicalTrials.gov