Evaluation of Pain Before and After Removal of Non-obstructive Kidney Stones

NCT03657667 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2023-04-04

No results posted yet for this study

Summary

Pain associated with renal stone disease is typically caused by an obstructing stone that obstructs the flow of urine, which results in renal collecting system dilatation. Non-obstructing renal calculi that do not cause renal collecting system dilatation are thought to be painless. The objective of this study is to prospectively determine if the removal of non-obstructing renal calculi can reduce or eliminate participant's pain and/or improve their quality of life.

Conditions

  • Kidney Stone

Interventions

PROCEDURE

Ureteroscopy

Endoscopic removal of kidney stones

Sponsors & Collaborators

  • Brigham and Women's Hospital

    collaborator OTHER
  • Henry Ford Health System

    collaborator OTHER
  • Milton S. Hershey Medical Center

    collaborator OTHER
  • Baylor Scott and White Health

    collaborator OTHER
  • Indiana University

    collaborator OTHER
  • University of Minnesota

    collaborator OTHER
  • University of California, Davis

    collaborator OTHER
  • Vanderbilt University Medical Center

    collaborator OTHER
  • University of California, San Diego

    collaborator OTHER
  • University of California, Los Angeles

    collaborator OTHER
  • Mayo Clinic

    collaborator OTHER
  • Centre hospitalier de l'Université de Montréal (CHUM)

    lead OTHER

Principal Investigators

  • Naeem Bhojani, MD · Centre hospitalier de l'Université de Montréal (CHUM)

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-28
Primary Completion
2022-10-06
Completion
2023-03-09

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

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 NCT03657667 on ClinicalTrials.gov