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Kidney StoneNCT01812772

The Effect of Ureteric Stent Tethers on Patient Symptoms and Urinary Infection

A study testing Double J-stent with a long tether and Double J-stent without a long tether in people with Kidney Stone, run by Unity Health Toronto at 1 site in Canada.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

RESEARCH QUESTION Do ureteric stents with tethers, left in-situ for 1-2 weeks, increase the rate of stent bacterial colonization, urinary bacterial colonization and stent related lower urinary tract symptoms compared to stents without tethers? HYPOTHESIS We hypothesize that ureteral double-J stents with tethers… Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Kidney Stone
What is being tested?
Double J-stent with a long tether and Double J-stent without a long tether
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
11 participants
Where
1 siteCanada
Study dates
Mar 2013to Feb 2014
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age over 18 years
  • First presentation for ureteroscopy for this particular stone
  • Planned insertion of a double J-stent
  • Follow-up conducted at St. Michael's Hospital

Who cannot join

  • Age <18years
  • Preexisting stent in place
  • Bilateral ureteric stents to be inserted
  • Patients with congenital kidney anomalies (horseshoe kidney, ectopic kidney, etc.)
  • Patients with an indwelling foley catheter
  • Patients with neurogenic bladder, chronic prostatitis, painful bladder syndrome or interstitial cystitis
Show all 11Show fewer
  • Patients with a urinary diversion (ileal conduit, ileal neobladder)
  • Patient currently taking an α-blocker (alfuzosin, terazosin,tamsulosin, prazosin)
  • Active urinary tract infection or positive screening urine culture at preadmission
  • Pregnancy
  • Patients who will not be returning to St. Michael's Hospital for follow-up

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • St. Michael Hospital

    Toronto, Ontario, M5B 1W8

Other trials in Canada

About this study

Official title: The Effect of Ureteric Stent Tethers on Patient Symptoms, Stent Bacterial Colonization and Urinary Tract Infection

RESEARCH QUESTION Do ureteric stents with tethers, left in-situ for 1-2 weeks, increase the rate of stent bacterial colonization, urinary bacterial colonization and stent related lower urinary tract symptoms compared to stents without tethers?

HYPOTHESIS We hypothesize that ureteral double-J stents with tethers increase the rate of stent bacterial colonization, but do not increase the rate of urinary bacterial colonization or stent related lower urinary tract symptoms compared to stents without tethers when left in-situ for 1-2 weeks.

Read the detailed description

Two of the main issues surrounding the use of ureteral stents are stent related symptoms and bacterial colonization/urinary tract infection (UTI). To be useful, stent tethers must decrease the morbidity associated with stent removal and the cost to the health care system, while not increasing stent related symptoms or UTI. To our knowledge, the effect of leaving a stent tether on stent symptoms and bacterial colonization of the stent and urine has not been previously studied.

This is a single-centre, prospective, randomized, controlled trial. Patients eligible for recruitment into the study based on the inclusion and exclusion criteria will be provided with a consent form at the time of their initial appointment, when their ureteroscopy is being booked. Once consent is obtained, patients will be randomized (using random number table look-up) to receive either double-J stent placement with a tether (the Treatment Group) or double-J stent placement without a tether (the Control Group) following ureteroscopy. Randomization will occur prior to the commencement of ureteroscopy.

Patients will either have a double J-stent placed with or without a long tether attached. The double-J stents used in the treatment and control groups will be otherwise identical. All stents will be 6 French in diameter and 22-26 cm in length based on the patients' height. Sizing of stent length will be performed uniformly in the treatment and control group and will involve measuring ureteric length from the ureteropelvic junction to ureterovesical junction with a marked ureteral catheter. All patients will receive a single preoperative dose of prophylactic antibiotics (i.e., Ampicillin and Gentamicin or Ciprofloxacin).All patients will have a urine sample collected for culture and sensitivity at the start of the procedure.

Blinding will not be feasible during this trial due to the nature of the intervention. The urologist performing the procedure will clearly be aware of whether a tether is left on the stent. Similarly, patients will also be aware of whether a string tether is protruding from their urethral meatus or not. However, assessors of the compiled data and questionnaires will be blinded to the intervention.

Once enrolled in the study, patients will be given the Ureteral Stent Symptoms Questionnaire 1 (Pre Stent) to complete prior to undergoing ureteroscopy and stent insertion. This will allow us to establish baseline lower urinary tract symptoms.

After completion of ureteroscopy and stent insertion and upon discharge from the hospital all patients will be provided with the following:

  1. Diary sheets to record daily analgesic use
  2. A prescription for a standardized analgesic regimen including Percocet (1 tablet PO q6h prn, 20 tablets) to be taken as needed for pain control.
  3. An appointment for the first follow-up visit (in 7-14 days)

At the follow-up visit, a kidney, ureter and bladder (KUB) radiograph will be performed and patients will complete the Ureteral Stent Symptoms Questionnaire 2 (Stent insitu). The KUB x-ray will be reviewed to ensure the stent remained in appropriate position and did not migrate and that any residual stone fragments have passed. Next, all patients will have their stent removed. Patients in the control group will undergo cystoscopy under local anesthesia for stent removal and those the treatment group will have the stent removed by the tether. This distal curl or lower end (bladder) of the double-J stent, in all patients, will be sent to microbiology for culture to determine the rate of stent bacterial colonization. Of note, all patients in the control group will provide a mid-stream urine sample to be sent for culture and sensitivity testing, after cystoscopy and stent removal, while all patients in the treatment group will provide a urine sample after the stent is removed, so the tether does not contaminate the sample. This urine sample will allow us to establish the rate of bacteriuria.

Upon discharge from the Cystoscopy unit following stent removal all patients will return for a final follow-up with renal ultrasound approximately 4-6 weeks post-stent removal and will be given the Ureteral Stent Symptoms Questionnaire 3 (Post Stent) to complete.

Conditions
Kidney Stone
Being tested
Double J-stent with a long tether, Double J-stent without a long tether
Keywords
urinary stents, ureteroscopy
Medical subject headings
Kidney Calculi

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Double J-stent with a long tetherDevice

    Patients will receive a double-J stent placement with a long tether following ureteroscopy.

  • Double J-stent without a long tetherDevice

    Patients will receive a double-J stent placement without a long tether following ureteroscopy.

Study groups in NCT01812772
Study groupRoleWhat they receive
Double J-stent with a long tetherExperimentalFollowing ureteroscopy patients will have placed a double J-stent with a long tether.
Receives: Device: Double J-stent with a long tether
Double J-stent without a long tetherActive comparatorFollowing ureteroscopy patients will have a double J-stent placed without a long tether
Receives: Device: Double J-stent without a long tether

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. The difference in stent related lower urinary tract symptoms based on mean scores from the Ureteral Stent Symptoms questionnaires

    Measured: The Ureteral Stent Symptoms Questionnaires will be completed before the procedure, 1 week after the procedure and 1 month after the stent was removed (5 weeks post procedure)

Secondary outcomes (1)
  1. the rate of stent bacterial colonization

    Measured: 1 week post procedure

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted18 Mar 2013 (estimated)
  2. Study startMar 2013
  3. Primary completionFeb 2014
  4. Study completionFeb 2014

Why it stopped: Low enrollment

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
11 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01812772
Sponsor's protocol ID
10-370
Status last verified
Feb 2014
First submitted
14 Mar 2013
Last updated
21 May 2015
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A study testing Double J-stent with a long tether and Double J-stent without a long tether in people with Kidney Stone, run by Unity Health Toronto at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 21 May 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was stopped early (reason given: Low enrollment). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The difference in stent related lower urinary tract symptoms based on mean scores from the Ureteral Stent Symptoms questionnaires (time frame: The Ureteral Stent Symptoms Questionnaires will be completed before the procedure, 1 week after the procedure and 1 month after the stent was removed (5 weeks post procedure)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 May 2015.

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