Actively Recruiting

Phase Not Applicable
Age: 18Years - 80Years
All Genders
NCT06987877

Efficacy of Routine Saline Flushing in the Prevention of Nephrostomy Tube Obstructions: A Pilot Study

Led by Brigham and Women's Hospital · Updated on 2026-02-06

20

Participants Needed

1

Research Sites

64 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The investigators performing this research to study if routine flushing is necessary to prevent obstructions of a nephrostomy tube. This study will evaluate patients that have nephrostomy tube or will have nephrostomy tubes placed as part of their standard clinical care. If participants agree to participate in this study, participants will undergo randomized assignment to either continue to routinely flush the nephrostomy tube with normal saline or not to routinely flush the nephrostomy tube with normal saline. Participantswill be in the study for approximately 3 months if they decide to stay for the whole study.

CONDITIONS

Official Title

Efficacy of Routine Saline Flushing in the Prevention of Nephrostomy Tube Obstructions: A Pilot Study

Who Can Participate

Age: 18Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 to 80 years
  • Planned nephrostomy tube exchange or new nephrostomy tube placement with ongoing need for nephrostomy tube
Not Eligible

You will not qualify if you...

  • Current local infection
  • History of anaphylaxis to iodinated contrast
  • Pregnant or planning pregnancy during the study
  • Irreversible coagulopathy
  • Planned definitive treatment for nephrostomy tube indication before 12 weeks post-intervention
  • Planned routine tube exchange before 12 weeks after placement or exchange
  • Complete sensory loss below T10 dermatome

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Brigham and Women's Hospital

Boston, Massachusetts, United States, 02115

Actively Recruiting

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Research Team

Y

Yan Epelboym, MD, MPH

CONTACT

A

Austin Lai, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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