Forced Diuresis After Flexible Ureteroscopy for Medium-Sized Renal Stones

NCT ID: NCT07336485

Last Updated: 2026-01-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

2000 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-01

Study Completion Date

2025-07-01

Brief Summary

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This randomized controlled clinical trial evaluated whether furosemide-assisted forced diuresis during flexible ureteroscopy reduced the residual fragment rate and improved the stone-free rate after flexible ureteroscopy for management of medium sized renal stones measuring up to 30 millimeters. Adult patients undergoing flexible ureteroscopy for renal stones were randomized into two parallel groups: an experimental group that received intravenous furosemide during the procedure and a control group that received standard perioperative and postoperative care without furosemide. Stone-free status and residual fragments were assessed using non-contrast computed tomography performed four weeks after the procedure, and residual fragments were classified by fragment size. Secondary outcomes included operative time, length of hospital stay, postoperative complications, total urine output in the first 24 hours, and the need for additional treatments for significant residual stones.

Detailed Description

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Conditions

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Kidney Stones

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants were randomly assigned in a one-to-one ratio to receive either intravenous furosemide-assisted forced diuresis during flexible ureteroscopy or standard care without furosemide during flexible ureteroscopy.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Furosemide-Assisted Forced Diuresis During Flexible Ureteroscopy

During flexible ureteroscopy, participants received intravenous furosemide 40 milligrams total, divided into 20 milligrams administered 5 minutes after induction of anesthesia and 20 milligrams administered 30 minutes after the start of the procedure.

Group Type EXPERIMENTAL

Furosemide

Intervention Type DRUG

Intravenous furosemide was administered as a total dose of 40 milligrams during the procedure, divided into 20 milligrams given 5 minutes after induction of anesthesia and 20 milligrams given 30 minutes after the start of the procedure.

Standard Care During Flexible Ureteroscopy Without Furosemide

Participants underwent flexible ureteroscopy and received standard perioperative and postoperative care without receiving intravenous furosemide or any other diuretic medication.

Group Type ACTIVE_COMPARATOR

Standard Care After Flexible Ureteroscopy Without Furosemide

Intervention Type OTHER

Participants received standard perioperative and postoperative management after flexible ureteroscopy without administration of furosemide or any other diuretic medication.

Interventions

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Furosemide

Intravenous furosemide was administered as a total dose of 40 milligrams during the procedure, divided into 20 milligrams given 5 minutes after induction of anesthesia and 20 milligrams given 30 minutes after the start of the procedure.

Intervention Type DRUG

Standard Care After Flexible Ureteroscopy Without Furosemide

Participants received standard perioperative and postoperative management after flexible ureteroscopy without administration of furosemide or any other diuretic medication.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Adult patients aged 18 years or older.
* Patients who underwent flexible ureteroscopy for renal stones measuring 30 millimeters or less.

Exclusion Criteria

* Patients with active urinary tract infection.
* Patients with a history of previous open renal surgery or renal trauma.
* Patients with contraindications to anesthesia, such as severe cardiac disease, uncontrolled diabetes mellitus, or severe coagulation disorder.
* Patients with severe renal impairment, defined as an estimated glomerular filtration rate less than 30 milliliters per minute per 1.73 square meters.
* Patients with a single kidney.
* Patients with contraindications to furosemide administration.
* Patients with congenital renal anomalies.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

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Ahmed Nasser Karamany Mokhat

Resident of Urology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Ain Shams University Hospitals (Urology Department)

Cairo, Cairo Governorate, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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FMASU MS 685/2025

Identifier Type: -

Identifier Source: org_study_id

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