Kidney Stone Clinical Trial
— FIREStonesOfficial title:
FIRESTONES : Impact of Forced Diuresis on the Residual Fragment Rate After Flexible Ureteroscopy for Destruction of Kidney Stones With Laser: a Randomized Controlled Two-parallel Group Multicenter Trial With Blinding Evaluation
In view of the positive results of the numerous studies conducted on forced diuresis after extra-corporeal lithotripsy, the investigators chose to evaluate forced diuresis by injection of Furosemide associated with intravenous hydration, which has never before been the subject of a specific analysis.
Status | Not yet recruiting |
Enrollment | 374 |
Est. completion date | March 15, 2026 |
Est. primary completion date | March 15, 2026 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility | Inclusion Criteria: - Patients = 18 years old and < 80 years old - With the need to perform a flexible ureteroscopy with destruction of the kidney stones with laser - Participants covered by or entitled to social security - Written informed consent obtained from the participant - Ability for participant to comply with the requirements of the study Exclusion Criteria: - Persons covered by articles L1121-5 to L1121-8 of the CSP (corresponding to all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial or administrative decision, minors, and persons subject to a legal protection measure: guardianship or trusteeship) - Contra-indication to Furosemide: - Hyper-sensitivity to the active substance or one of the excipients - Hyper-sensitivity to Sulfonamide - Renal failure with oligo-anuria refractory to Furosemide - Hypokalemia < 3,5 mmol/L - Severe hyponatremia - Hypovolemia with or without hypotension or dehydration - Ongoing hepatitis, hepatic insufficiency severe and hepatic encephalopathy - Patient having Furosemide as usual treatment - Patient requiring an injection of Aminoside or Vancomycin before or during the procedure - Participation in other interventional research with an investigational drug or medical device |
Country | Name | City | State |
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n/a |
Lead Sponsor | Collaborator |
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University Hospital, Tours |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Rate of stone free patients | Rate of stone-free patients 3 months after a flexible ureteroscopy for renal stone laser destruction, evaluated on the low dose abdomino-pelvic CT-Scan.
A centralized review of the images will be performed by two specialized radiologists, in a blind and crossed way to allow a homogenization of the results |
At 3 months | |
Secondary | Rate of urinary infection | Rate of post-operative urinary tract infection will be assessed within 30 days after surgery on the combination of:
Fever higher than 38.5°C and/or, Chills and/or, Clinical symptoms (supra-pubic pain, dysuria, pollakiuria, urgency, urinary burning, back pain radiating to the genitals, hematuria) and/or Positive urine culture with a significant bacteriuria threshold defined as bacteriuria =10^5 UFC/mL with one or two bacterial species. |
From baseline to 30 days | |
Secondary | Pain in a scale | Post-operative pain will be assessed on numerical pain scale in the recovery room, in the service and at the discharge. Pain scale is from 0 (no pain) to 10 (as bad as it could be nothing else matters) | During the hospital stay | |
Secondary | Opioid consumption | The use of opioids will be reported | During the hospital stay, an average of 1 day | |
Secondary | Number of participants with adverse events | Number of participants with Furosemide adverse events | From baseline to 3 months, an average of 1 day |
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