- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00739284
A Prospective Comparison Between Ureteral Stent and Nephrostomy Tube for an Urgent Drainage of Obstructed Kidney (JJVsPCN08)
August 20, 2008 updated by: Rabin Medical Center
Kidney obstruction might be caused by a stone in the urinary tract.
In case of accompanying fever or renal failure, an urgent drainage might be needed.
This can be done either by placing an ureteral stent or a nephrotomy tube.
Only limited number of studies examined the question which of the two is preferred.
A debate exist regarding the effectiveness of each procedure to improve symptoms, renal function and treating an infection.
Our goal is to resolve this debate and to state whether one way is preferred on the other.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Shay Golan, MD
- Phone Number: 972-3-9376560
- Email: shayg@clalit.org.il
Study Locations
-
-
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Petach Tikva, Israel
- Recruiting
- Rabin Medical Center
-
Contact:
- Shay Golan, MD
- Phone Number: 972-3-9376560
- Email: shayg@clalit.org.il
-
Principal Investigator:
- Shay Golan, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria: Patient suffering from obstructed kidney by a stone and at least one of these situations:
- fever (above 38c)
- A rise in creatine to above 1.5
- Pain resistent to multiple analgetic treatments
Exclusion Criteria:
- Patients with medical condition that prevent the use of one of the procedures
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
---|
quality of life
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2008
Primary Completion (ANTICIPATED)
August 1, 2008
Study Registration Dates
First Submitted
August 20, 2008
First Submitted That Met QC Criteria
August 20, 2008
First Posted (ESTIMATE)
August 21, 2008
Study Record Updates
Last Update Posted (ESTIMATE)
August 21, 2008
Last Update Submitted That Met QC Criteria
August 20, 2008
Last Verified
August 1, 2008
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- JJVsPCN08
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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