Ignite Creation Date:
2024-05-05 @ 11:51 AM
Last Modification Date:
2024-10-26 @ 9:14 AM
Study NCT ID:
NCT00151567
Status:
COMPLETED
Last Update Posted:
2012-12-04
First Post:
2005-09-08
Brief Title:
Evaluation of Tamsulosin in the Treatment of Ureteral Stones
Sponsor:
Rennes University Hospital
Organization:
Rennes University Hospital
Study Overview
Official Title:
Interest of a Treatment With the alpha1-blocker Tamsulosin in the Elimination of Pelvis Ureteral Stones
Status:
COMPLETED
Status Verified Date:
2008-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
TAMSULOSINE
Brief Summary:
Ureteral stones have an important place in daily urological practice usually causing acute episodes of ureteral colic by obstructing the urinary tract The aim of the study is to evaluate whether repeated administration of tamsulosin a drug routinely used in the treatment of lower urinary tract symptoms could lower the delay of elimination of the stone in patients with pelvis ureterolithiasis
Detailed Description:
Ureteral colic mainly due to ureterolithiasis represents 1 to 2 of hospital emergency admissions When a surgical intervention is not required usual treatment combines hydration and anti-inflammatory drugs
Alpha1-blockers firstly developed as anti-hypertensive drugs are now also used in the management of benign prostatic hyperplasia due to their relaxing properties on the urinary tract The aim of the study is to investigate whether tamsulosin could lower the delay of elimination of the stone in patients with pelvis ureterolithiasis Patients are randomized to receive either tamsulosin or a placebo in addition to usual treatment until stone elimination Efficacy is assessed by evaluating the time to spontaneous passage of the stone between day 1 and day 42 the need for surgery and pain recurrences
Alpha1-blockers firstly developed as anti-hypertensive drugs are now also used in the management of benign prostatic hyperplasia due to their relaxing properties on the urinary tract The aim of the study is to investigate whether tamsulosin could lower the delay of elimination of the stone in patients with pelvis ureterolithiasis Patients are randomized to receive either tamsulosin or a placebo in addition to usual treatment until stone elimination Efficacy is assessed by evaluating the time to spontaneous passage of the stone between day 1 and day 42 the need for surgery and pain recurrences
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| CIC0203004 | Other Identifier | Rennes University Hospital | None |
| PHRC00-01 | OTHER | None | None |