Tumor Clinical Trial
Official title:
The Impact of Ureteral Stents on Peristalsis
NCT number | NCT01739738 |
Other study ID # | H12-03027 |
Secondary ID | |
Status | Withdrawn |
Phase | |
First received | |
Last updated | |
Start date | December 2012 |
Est. completion date | December 2014 |
Verified date | March 2020 |
Source | University of British Columbia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The purpose of the study is to investigate the impact of ureteral stents on the functioning of ureteral peristalsis (normal contractions in the ureteral organ muscle).
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | December 2014 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 19 Years and older |
Eligibility |
Inclusion Criteria: 1. stone disease 2. localized tumor disease 3. hydronephrosis of unknown ethiology 4. patients who receive a prophylactic stent before a planned operation. Exclusion Criteria: 1. Patients being septic and in a life-threatening condition before or after stent-insertion 2. patients with tumors in a progressive state that affect the retroperitoneum (contralateral ureter might be affected and can not serve as a control for the stented side) 3. patients with Morbus Ormond (same reason as above) 4. patients requiring ureteral stents bilaterally (same reason as above) 5. long-term stented patients will be excluded as we are interested in evaluating the onset of changes in peristalsis rate which are expected to be most significant in an acute setting. 6. patients with preexisting abnormalities/pathologies of the urinary tract e.g. reflux disease, megaureter or bladder dysfunctions as these will likely affect our results 7. non English-speaking patients will be excluded as they will not be able to understand the letter of consents. Exclusion criteria for control group: 1. known preexisting pathology in the urinary tract (see above) 2. volunteers who underwent previous surgical procedures on kidney, ureter or bladder within the past 5 years as this may change the starting position of our study 3. patients currently taking an a-blocker (alfuzosin, terazosin, doxazosin, tamsulosin, prazosin) because these medications are known to affect peristalsis 4. patients currently taking calcium channel blocker (verapamil, diltiazem, nifedipine, nicardipine, bepridil, mibefradil) because these medications are known to affect peristalsis |
Country | Name | City | State |
---|---|---|---|
Canada | University of British Columbia/Vancouver General Hospital | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
University of British Columbia |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Effect of stent on ureteral peristalsis in stented ureter | before and after stent insertion (approximately 30 minutes) | before and after stent insertion (approximately 30 minutes) | |
Secondary | Effect of stent on ureteral peristalsis in non-stented ureter | Effect of stent on ureteral peristalsis in non-stented ureter pre and post stenting | 30 minutes (pre and post stenting) |
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