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Magnetic Ureteral Stent Symptoms - a Comparison to Standard Ureteral Stent as Perceived By the Patient (MAGUSS) (MAGUSS)

Primary Purpose

Urinary Tract Stone, Kidney Stone

Status
Unknown status
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
ureteral double-J stent removal using magnet
ureteral double-J stent removal using cystoscopy
Sponsored by
Turku University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Tract Stone focused on measuring Urinary tract stone, ureter double-J stent

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Language spoken: Finnish
  • Clinically evaluated need for short term ureter stenting in course of extracorporeal shockwave lithotripsy-treatment or after pyeloscopy
  • Mental status: Patients must be able to understand the meaning of the study
  • Informed consent: The patient must sign the appropriate Ethics Committee (EC) approved informed consent documents in the presence of the designated staff

Exclusion Criteria:

  • Current use of alpha blockers
  • Patients undergoing emergency ureteroscopy and stenting
  • Patients with a long term ureter stents
  • Any other conditions that might compromise patients safety, based on the clinical judgment of the responsible urologist

Sites / Locations

  • Keski-Suomi Central HospitalRecruiting
  • Satakunta Central HospitalRecruiting
  • Turku University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Magnetic double-J ureteric stent

Standard double-J ureteric stent

Arm Description

Double-J ureteric stent removed using magnet

Double-J stent removed using cystoscopy

Outcomes

Primary Outcome Measures

Change in Pain score in Ureteral Stent Symptom Questionnaire (USSQ)
4 weeks after stent placement. [5] Less than 5 points of difference between the two study groups is considered as clinically insignificant.

Secondary Outcome Measures

General health score in Ureteral Stent Symptom Questionnaire (USSQ)
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Sexual score in Ureteral Stent Symptom Questionnaire (USSQ)
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Working performance score in Ureteral Stent Symptom Questionnaire (USSQ)
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Urinary symptom score in Ureteral Stent Symptom Questionnaire (USSQ)
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.

Full Information

First Posted
August 2, 2017
Last Updated
October 7, 2021
Sponsor
Turku University Hospital
Collaborators
Kuopio University Hospital, Satakunta Central Hospital, Jyväskylä Central Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03257306
Brief Title
Magnetic Ureteral Stent Symptoms - a Comparison to Standard Ureteral Stent as Perceived By the Patient (MAGUSS)
Acronym
MAGUSS
Official Title
Magnetic Ureteral Stent Symptoms - a Comparison to Standard Ureteral Stent as Perceived By the Patient (MAGUSS)
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 9, 2018 (Actual)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Turku University Hospital
Collaborators
Kuopio University Hospital, Satakunta Central Hospital, Jyväskylä Central Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The specific aim of this study is to validate our hypothesis that the magnetic ureteral stents have the same amount of adverse effects as the more commonly used non-magnetic ureteral stents. If this hypothesis would be confirmed then the usage of magnetic ureteral stents would be justified for both reducing patient discomfort by way of fewer cystoscopies and possibly also decreasing the overall expenditures of treatment.
Detailed Description
Many urological procedures involving the kidney and the ureters require a stent replacement to avoid un-wanted adverse invents caused by the procedure itself. The stenting, however, predisposes the patient to adverse effects of its own and the application and removal of the stent is a notable monetary expense. The use of magnetic ureteral stents that can be removed via catheter instead of requiring an additional cystoscopy for removal would reduce the discomfort to patients and also possibly decrease the expenditures of the overall treatment. However, the comparability of standard ureteral stents and the magnetic ureteral stents is largely unknown due to there being no published research on the subject as of this time. The specific aim of this study is to validate our hypothesis that the magnetic ureteral stents have the same amount of adverse effects as the more commonly used non-magnetic ureteral stents. The design is as prospective randomized, single-blinded, multi-institutional, non-inferiority study conducted in Hospital Districts of Southwest Finland, Päijät-Häme, Pohjois-Savo, Satakunta and Keski-Suomi. Using age and gender stratification, patients are randomised 1:1 fashion into having a magnetic (n=85) or standard ureter stent (n=85). The primary objectives are the mean differences between the two groups in pain and urinary symptoms scores determined by the Ureteral Stent Symptom Questionnaire (USSQ) 4 weeks after stent placement. The patients will be recruited starting from the 4rd quarter of 2018 and ending during the 3rd quarter of 2020. Preliminary analysis of all results will be available in September 2020 and reports are expected to be written during December 2020.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Tract Stone, Kidney Stone
Keywords
Urinary tract stone, ureter double-J stent

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Prospective randomized, single-blinded, multi-institutional, non-inferiority study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
170 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Magnetic double-J ureteric stent
Arm Type
Active Comparator
Arm Description
Double-J ureteric stent removed using magnet
Arm Title
Standard double-J ureteric stent
Arm Type
Active Comparator
Arm Description
Double-J stent removed using cystoscopy
Intervention Type
Procedure
Intervention Name(s)
ureteral double-J stent removal using magnet
Intervention Description
Double-J ureteric stent removed using magnet
Intervention Type
Procedure
Intervention Name(s)
ureteral double-J stent removal using cystoscopy
Intervention Description
Double-J ureteric stent removed using cystoscopy
Primary Outcome Measure Information:
Title
Change in Pain score in Ureteral Stent Symptom Questionnaire (USSQ)
Description
4 weeks after stent placement. [5] Less than 5 points of difference between the two study groups is considered as clinically insignificant.
Time Frame
4 weeks after stent placement and 4 weeks after stent removal
Secondary Outcome Measure Information:
Title
General health score in Ureteral Stent Symptom Questionnaire (USSQ)
Description
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Time Frame
4 weeks after stent placement and 4 weeks after stent removal
Title
Sexual score in Ureteral Stent Symptom Questionnaire (USSQ)
Description
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Time Frame
4 weeks after stent placement and 4 weeks after stent removal
Title
Working performance score in Ureteral Stent Symptom Questionnaire (USSQ)
Description
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Time Frame
4 weeks after stent placement and 4 weeks after stent removal
Title
Urinary symptom score in Ureteral Stent Symptom Questionnaire (USSQ)
Description
4 weeks after stent placement. Scores less than 4 points of difference between the two study groups is considered as clinically insignificant.
Time Frame
4 weeks after stent placement and 4 weeks after stent removal
Other Pre-specified Outcome Measures:
Title
The discomfort experienced by the patients during stent removal determined in 100mm Visual Analogue Scale (VAS).
Description
More than 10mm difference between the two groups is considered as clinically significant.
Time Frame
4 weeks after stent placement
Title
The number of unsuccessful removals of the magnetic stent.
Description
Unsuccessful removal using magnet
Time Frame
4 weeks after stent placement

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Language spoken: Finnish Clinically evaluated need for short term ureter stenting in course of extracorporeal shockwave lithotripsy-treatment or after pyeloscopy Mental status: Patients must be able to understand the meaning of the study Informed consent: The patient must sign the appropriate Ethics Committee (EC) approved informed consent documents in the presence of the designated staff Exclusion Criteria: Current use of alpha blockers Patients undergoing emergency ureteroscopy and stenting Patients with a long term ureter stents Any other conditions that might compromise patients safety, based on the clinical judgment of the responsible urologist
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kari T Syvänen, MD, PhD
Phone
+3582313000
Email
kari.syvanen@tyks.fi
First Name & Middle Initial & Last Name or Official Title & Degree
Otto Ettala, MD, PhD
Phone
+3582313000
Email
otto.ettala@tyks.fi
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kari T Syvänen, MD, PhD
Organizational Affiliation
Turku University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Keski-Suomi Central Hospital
City
Jyväskylä
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Heikki Seikkula, MD, PhD
Email
heikki.seikkula@ksshp.fi
Facility Name
Satakunta Central Hospital
City
Pori
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Teemu Joutsi, MD
Email
teemu.joutsi@satshp.fi
First Name & Middle Initial & Last Name & Degree
Lauri Reunanen, MD
Facility Name
Turku University Hospital
City
Turku
ZIP/Postal Code
20521
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kari T Syvänen, MD, PhD
Phone
+3582313000
Email
kari.syvanen@tyks.fi
First Name & Middle Initial & Last Name & Degree
Otto Ettala, MD, PhD
Phone
+3582313000
Email
otto.ettala@tyks.fi

12. IPD Sharing Statement

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Magnetic Ureteral Stent Symptoms - a Comparison to Standard Ureteral Stent as Perceived By the Patient (MAGUSS)

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