Ureteral Stent Length and Patient Symptoms

This study has been terminated.
(Because no staff to consent or enroll subjects)
Sponsor:
Information provided by (Responsible Party):
John G Pattaras, MD, Emory University
ClinicalTrials.gov Identifier:
NCT00288457
First received: February 6, 2006
Last updated: December 23, 2013
Last verified: December 2013

February 6, 2006
December 23, 2013
February 2006
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Complete list of historical versions of study NCT00288457 on ClinicalTrials.gov Archive Site
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Ureteral Stent Length and Patient Symptoms
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The Study of whether or not Ureteral Stent Length affects patient comfort after electro-shock wave treatment for kidney stones.

Patients undergoing electro shock wave for treatment of kidney stones are randomized to long or short stent length after signing an informed consent prior to their surgery. They keep a pain diary and medication diary for a two week period after the stent is placed. These are turned in at the two week post-op visit. Patients also complete a quality of life and urinary symptom score questionnaire pre and post operatively.

Observational
Time Perspective: Prospective
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Probability Sample

Male or female over 18 years of age, will be receiving electro-shock wave therapy for kidney stones

Kidney Stones
Device: Ureteral Stent
Ureteral stents are not investigatory but rather part of standard of care. In this study, we were interested in having patients fill out pre and post-operative questionnaires so that we could compare their symptoms with the length of their ureter and the stent placed.
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
1
October 2006
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Inclusion Criteria: Male or female over 18 years of age, will be receiving electro-shock wave therapy for kidney stones -

Exclusion Criteria:Under 18 years of age, inability to give informed consent

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Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
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NCT00288457
0758-2003
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John G Pattaras, MD, Emory University
Emory University
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Principal Investigator: John G Pattaras, MD Emory University
Emory University
December 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP