Effectiveness of Drainage by PCN vs. JJ in Patients With Symptoms of Obstructive Kidney Disease Caused by Urolithiasis
NCT ID: NCT04594161
Last Updated: 2024-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
204 participants
INTERVENTIONAL
2020-07-15
2024-01-01
Brief Summary
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Detailed Description
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Hypothesis: Percutaneous nephrostomy is non inferior to retrograde double J catheter regarding time to clinical recovery. Secondly, patient reported outcome measures (PROMS) comparing treatment room and OR settings of drainage procedures will most likely not be significantly different.
Finally, because percutaneous nephrostomy catheters are more often placed in a (outpatient) urological or radiological treatment room, this is expected to be less expensive than placement of a double J catheter (more often placed in the OR). Objective: To investigate the effectiveness of percutaneous nephrostomy catheter placement versus retrograde double J catheter placement in patients with symptoms of obstructive kidney disease (with either infection and/or pain and/or kidney function deterioration) caused by urolithiasis.
Study design: Multicenter prospective randomized controlled non-inferiority trial.
Study population: Male and female adult patients with signs of obstructive kidney disease with kidney or ureteral lithiasis as an underlying cause and with an indication for drainage based on symptoms of or laboratory tests indicating infection and/or pain and/or kidney function.
Intervention: One group receives drainage by percutaneous nephrostomy catheter placement as opposed to the other group which will receive drainage by retrograde double J catheter placement.
Main study parameters/endpoints:
The primary objective is to assess whether a PCN is non-inferior to double J catheter regarding time to clinical recovery in patients with obstructive kidney disease resulting from urolithiasis.
The primary outcome parameter is time to clinical recovery. Clinical recovery is defined as reaching one or more of the following criteria. The mandatory amount of criteria to achieve clinical recovery is dependent on the indication for placement of a PCN or a JJ.
* If indication for drainage is infection: improvement of infection, indicated by a decrease of WBC in two executive laboratory results and below 15.000 mm3 and a body temperature of 36-38.5 C. and/or
* If indication for drainage is untreatable pain: Numeric rating score (NRS) considering pain resulting from a renal colic is improved and \< 3 points and/or
* If indication for drainage is deterioration of kidney function: improvement of creatinine/ Glomerular Filtration Rate (GFR) in two executive laboratory results It may occur that the indication for drainage is a combination of the above named indications. Clinical recovery will then be reached in case all parameters related to the different indications are within the set range. Secondary outcomes are further clinical data, PROMS (measured by the EQ-5D-5L, NRS, a satisfaction scale and a catheter questionnaire) and societal costs (measured by a diseasespecified iMCQ questionnaire).
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: The placement of either PCN or double J catheter is standard care. Currently the choice for PCN or a double J catheter is based on expert opinion and may be driven by arguments considering logistics or assumptions about the quality of life for a patient after placement.
Considering the difference in rate of placement of both PCN and double J catheter between various hospitals and different countries, it is believed experts have no uniform work method to handle the dilemma of choosing between these two techniques.\[2\] Furthermore the current EAU-guideline 2018 states that both methods of drainage are to be considered as equal.\[1\] Therefore there is no reason to believe, patients will be affected negatively by being placed randomly in either the double J group or the PCN group. Questionnaires will be filled in daily during hospitalization and twice or less afterwards. This is not considered to be a risk for the patient. The longest questionnaires (EQ-5D-5L and iMCQ) will take approximately 10-20 minutes to fill in, additional to the shorter scales (NRS, satisfaction scale) which will take approximately 1 minute to fill in. Generally It will take 90 minutes, spread over the course of three months, to fill in all questionnaires. For frequency and timing of the questionnaires. Finally, no additional visits to a hospital, withdrawal of blood samples or exposure to radiation is to be expected when taking part in this study.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
OTHER
NONE
Study Groups
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Percutaneous Nephrostomy
drainage of the kidney by means of a percutaneous Nephrostomy
Percutaneous Nephrostomy
A Percutaneous Nephrostomy will be placed in patients with obstructive urolithiasis
Double J catheter
drainage of the kidney by means of a double J catheter
Double J catheter
A Double J catheter will be placed in patients with obstructive urolithiasis
Interventions
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Percutaneous Nephrostomy
A Percutaneous Nephrostomy will be placed in patients with obstructive urolithiasis
Double J catheter
A Double J catheter will be placed in patients with obstructive urolithiasis
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Male/female \>18 year
* Symptoms and/or laboratory results indicating obstructive kidney disease with or without infection.
* A kidney or ureteral stone is present on ultrasound or CT (max 3 months old prior to presentation)
* Both drainage techniques are feasible and safe in opinion of the treating physician (from logistics point of view and in the best interest of the patient).
* Willing and able to comply with filling in questionnaires and follow-up regiment
Exclusion Criteria
* Analphabetic or not mastering the Dutch language
* Pregnancy
* Usage of anticoagulation agents other than acetylsalicylic acid.
* Contraindication for either technique looking at history and anatomy (e.g. kidney transplant, pouch, Bricker deviation, urethral or ureteral stenosis)
ALL
No
Sponsors
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Alrijne Hospital
OTHER
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
OTHER
Responsible Party
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Prof.dr. H.P. Beerlage
Professor doctor H.P. Beerlage
Principal Investigators
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Ad Hendrikx, dr.
Role: STUDY_CHAIR
no affiliation
Locations
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Amsterdam UMC, location AMC
Amsterdam, North Holland, Netherlands
Countries
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Related Links
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official dutch website
Other Identifiers
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NL70822.058.19
Identifier Type: OTHER
Identifier Source: secondary_id
METC 2020_057
Identifier Type: -
Identifier Source: org_study_id
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