TOTEME: Tolerance and Effectiveness of Ureteral Stents MEMOKATH ® 051 in Chronic Strictures of the Ureter

Sponsor
University Hospital, Bordeaux (Other)
Overall Status
Completed
CT.gov ID
NCT00790686
Collaborator
(none)
13
4
1
53.9
3.3
0.1

Study Details

Study Description

Brief Summary

TOTEME offers to treat certain chronic strictures of the ureter with MEMOKATH 051 to assess its effectiveness, tolerance and mean durability during a 3 years follow up period.

Patients usually treated with double J stents will be included. The double J stent will be replaced by a MEMOKATH 051 stent under general anesthesia during a cystoscopy. After this procedure, the patients will have medical examinations, blood exams, radiography and renal sonography during 3 years. If a problem of tolerance or effectiveness is diagnosed, the ureteral stent MEMOKATH 051 will be changed or replaced with a double J stent.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Insertion of Memokath 051
Phase 2

Detailed Description

Introduction:

The chronic strictures of the ureter are usually treated by double J stents. They allow the emptying of the kidney and avoid the deterioration of renal function. Unfortunately, double J stents have to be replaced every 6 month and are at the origin of irritative lower urinary tract symptoms and lumbar pain which corrupt the quality of life of the patients.

Ureteral stricture could also be treated with MEMOKATH 051. These new ureteral stents seem not to require iterative changes and also not to cause irritative symptoms and lumbar pain. MEMOKATH 051 could therefore allow to reduce the number of changes and to ameliorate the quality of life of the patients.

Main objective:

Main objective is to assess effectiveness and tolerance of the MEMOKATH ® 051 in the treatment of chronic strictures of the ureter.

Resume:

Patients usually treated with double J stents will be included. The double J stent will be replaced by a MEMOKATH 051 stent under general anesthesia during a cystoscopy.

After this procedure, the patients will have medical examination, blood exams, radiography and renal sonography at 1 month, 3 month and every 6 month during a 3 years follow up period.

If a problem of tolerance or effectiveness is diagnosed, the ureteral stent MEMOKATH 051 will be changed or replaced with a double J stent and an adverse event will be declared.

Study Design

Study Type:
Interventional
Actual Enrollment :
13 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Study of Tolerance and Effectiveness of Ureteral Stents MEMOKATH ® 051 in the Treatment of Chronic Strictures of the Ureter
Study Start Date :
Nov 1, 2008
Actual Primary Completion Date :
May 1, 2013
Actual Study Completion Date :
May 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: 1

Memokath 051

Procedure: Insertion of Memokath 051
Patients usually treated with double J stents will be included. The double J stent will be replaced by a MEMOKATH 051 stent under general anesthesia during a cystoscopy.

Outcome Measures

Primary Outcome Measures

  1. Average durability of the stent MEMOKATH ® 051 [3 years]

Secondary Outcome Measures

  1. Proportion of ureteral stent MEMOKATH ® 051 positioning failure [3 years]

  2. Average quality of life of the patients measured by auto-questionary [3 years]

  3. Proportion of patients to which the ureteral stent was definitely taken away [3 years]

  4. Expense of hospitalizations for replacement of the ureteral stent [3 years]

  5. Proportion of replacement of the ureteral stent [3 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18-year-old or superior

  • Chronic stenosis of the ureter treated by placement of a ureteral endoprosthesis for more than six months;

  • No possibility for surgical or endoscopic treatment of the ureteral stricture

  • Free Consent, dated and signed by the patient

  • Affiliated Subject of a regime of French national health and pensions organization.

Exclusion Criteria:
  • Age under 18 year old

  • Pregnant or nursing Women

  • Patient having a life expectancy of less than 1 year

  • Patient having unique kidney

  • Patient having severe renal insufficiency (creatinin clearance under 30 ml/min)

  • Possible surgical or endoscopic treatment of ureteral stricture

  • Repeated urinary tract stones

  • Urothelial tumor of the bladder

  • Retro peritoneal fibrosis in the course of evolution

  • Complications of double J stents requiring more thanks a lot every 6 months

  • Against anaesthetic indication

  • Lithiasic inlay probe Double J with obstruction within 6 months

  • Persons put under maintenance of justice

  • Persons in inability to understand the sequence of try

Contacts and Locations

Locations

Site City State Country Postal Code
1 Department of Urology, University Hospital, Bordeaux Bordeaux France 22076
2 Department of Urology, University Hospital, Limoges Limoges France 87042
3 Department of Urology, Hospices Civils de Lyon Lyon France 69437
4 Department of Urology, University Hospital, Toulouse Toulouse France 31059

Sponsors and Collaborators

  • University Hospital, Bordeaux

Investigators

  • Principal Investigator: Gregoire Robert, MD, University Hospital, Bordeaux
  • Study Chair: Antoine BENARD, MD, University Hospital, Bordeaux

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Bordeaux
ClinicalTrials.gov Identifier:
NCT00790686
Other Study ID Numbers:
  • CHUBX2008/24
First Posted:
Nov 13, 2008
Last Update Posted:
Aug 21, 2014
Last Verified:
Aug 1, 2014
Keywords provided by University Hospital, Bordeaux
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 21, 2014