Ureteral Stent Length and Patient Symptoms
Sponsor
Emory University (Other)
Overall Status
Terminated
CT.gov ID
NCT00288457
Collaborator
(none)
1
8
Study Details
Study Description
Brief Summary
The Study of whether or not Ureteral Stent Length affects patient comfort after electro-shock wave treatment for kidney stones.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
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.
Study Design
Study Type:
Observational
Actual Enrollment
:
1 participants
Time Perspective:
Prospective
Study Start Date
:
Feb 1, 2006
Actual Study Completion Date
:
Oct 1, 2006
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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
-
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Emory University
Investigators
- Principal Investigator: John G Pattaras, MD, Emory University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
John G Pattaras, MD,
Associate Professor,
Emory University
ClinicalTrials.gov Identifier:
NCT00288457
Other Study ID Numbers:
- 0758-2003
First Posted:
Feb 8, 2006
Last Update Posted:
Dec 24, 2013
Last Verified:
Dec 1, 2013
Additional relevant MeSH terms: