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NCT Number: NCT07798336

6.3Fr Versus 7.5Fr Mini-Flexible Ureteroscopy for Renal Stones (MINI-FURS)

This prospective, randomized, single-blinded, non-inferiority clinical trial will compare the clinical outcomes and cost-effectiveness of two mini-flexible ureteroscopes (6.3Fr and 7.5Fr) used during flexible ureteroscopy for the treatment of renal stones. Adult patients with renal stones up to 15 mm who are scheduled to undergo flexible ureteroscopy will be randomly assigned to one of the two study groups. The primary objectives are to compare stone-free rates and the ability to achieve primary renal access without preoperative ureteral stenting. Secondary outcomes include operative time, fluoroscopy use, ureteral trauma, postoperative stenting, pain, complications, emergency department visits, need for additional procedures, hospital stay, and cost-effectiveness. The results of this study are expected to provide high-quality evidence to guide the selection of mini-flexible ureteroscopes and improve the quality, safety, and value of surgical care for patients with kidney stones.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sault Area Hospital

Sault Ste. Marie, Ontario, P6B 0A8, Canada

Location contact

Ali O Abdelhady, MD

CONTACT

[email protected]

5042664549

Ali O Abdelhady, MD

SUB_INVESTIGATOR

Yasser A Noureldin, MD, PhD (Urol), FEBU, FACS

CONTACT

[email protected]

416-318-2239

Yasser A Noureldin, MD, PhD (Urol), FEBU, FACS

PRINCIPAL_INVESTIGATOR

About this study

Renal stone disease is a common condition with an increasing global incidence. Flexible ureteroscopy has become one of the standard treatments for renal stones because it provides excellent stone clearance with a minimally invasive approach. Recent technological advances have led to the development of mini-flexible ureteroscopes with smaller diameters, which may facilitate easier access to the kidney while reducing ureteral trauma and the need for preoperative ureteral stenting.

Although both 6.3Fr and 7.5Fr mini-flexible ureteroscopes are currently available for clinical use, there is limited high-level evidence comparing their clinical performance and cost-effectiveness. This prospective, randomized, single-blinded, non-inferiority trial aims to compare these two ureteroscope sizes in adult patients undergoing flexible ureteroscopy for renal stones.

Eligible participants will be randomized in a 1:1 ratio to undergo flexible ureteroscopy using either a 6.3Fr or a 7.5Fr mini-flexible ureteroscope. All procedures will be performed using standardized surgical techniques by experienced endourologists.

The primary outcomes are stone-free rate at one month after surgery and successful primary renal access without preoperative ureteral stenting. Secondary outcomes include operative time, fluoroscopy utilization, intraoperative ureteral trauma, postoperative ureteral stenting, postoperative pain, complications classified using the Clavien-Dindo system, emergency department visits, hospital length of stay, need for secondary procedures, and cost-effectiveness from the hospital payer perspective.

The investigators hypothesize that the 6.3Fr mini-flexible ureteroscope will improve primary renal access while reducing ureteral trauma, fluoroscopy exposure, postoperative stenting, and overall healthcare costs without compromising stone-free rates. The findings of this study may help establish evidence-based recommendations for selecting mini-flexible ureteroscopes and optimize the surgical management of patients with renal stone disease.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

* Adults aged 18 years or older.

  • Scheduled to undergo flexible ureteroscopy for renal stones.
  • Renal stone size ≤15 mm in the greatest dimension.
  • No indwelling ureteral stent at the time of surgery.
  • Able and willing to provide written informed consent.

Exclusion criteria

* Active urinary tract infection.

  • Anatomical abnormalities of the urinary tract (e.g., ureteral stricture, horseshoe kidney, ectopic kidney).
  • Solitary kidney.
  • Pregnancy.
  • Stones located within a calyceal diverticulum.
  • Any condition that, in the opinion of the investigator, would interfere with study participation or follow-up.

Treatment and study plan

6.3Fr Mini-Flexible Ureteroscope

Device

Use of a disposable 6.3Fr mini-flexible ureteroscope during flexible ureteroscopy for renal stone treatment

7.5Fr Mini-Flexible Ureteroscope

Device

Use of a disposable 7.5Fr mini-flexible ureteroscope during flexible ureteroscopy for renal stone treatment

Primary outcomes

  1. Stone Free Rate

    Time frame: 1 month after surgery

    Stone-free status defined as the absence of residual stone fragments greater than 2 mm on non-contrast CT KUB

  2. Primary Renal Access Success Rate

    Time frame: Perioperative/Periprocedural

    Successful passage of the flexible ureteroscope into the renal collecting system without the need for preoperative ureteral stenting

Secondary outcomes

  1. Operative Time

    Time frame: During surgery

    Total operative time measured from insertion of the ureteroscope until completion of the procedure

  2. Intraoperative Fluoroscopy Use

    Time frame: During surgery

    Fluoroscopy utilization during the procedure, including fluoroscopy time

  3. Intraoperative Ureteral Trauma as Assessed by the Traxer Ureteral Injury Scale

    Time frame: Perioperative/Periprocedural

    Ureteral trauma will be assessed using the Traxer Ureteral Injury Scale, graded from 0 to 3, where Grade 0 indicates no observable ureteral injury and Grade 3 indicates the most severe ureteral injury. Higher scores indicate greater severity of ureteral injury.

  4. Postoperative Ureteral Stenting Rate

    Time frame: Immediately after surgery

    Percentage of participants requiring ureteral stent placement at the end of surgery

  5. Postoperative Pain as Assessed by the Visual Analog Scale

    Time frame: 6, 24, and 48 hours after surgery

    Postoperative pain will be assessed using the Visual Analog Scale, ranging from 0 to 10, where 0 represents no pain and 10 represents the worst possible pain. Higher scores indicate greater pain.

  6. Postoperative Complications

    Time frame: Up to 30 days after surgery

    Complications graded using the Clavien-Dindo Classification

  7. Emergency Department Visits

    Time frame: Within 2 weeks after surgery

    Emergency department visits related to the procedure

  8. Hospital Length of Stay

    Time frame: Perioperative/Periprocedural period (from admission to discharge)

    Length of hospital stay measured in hours from admission for the index ureteroscopy procedure to hospital discharge.

  9. Need for Secondary Procedures

    Time frame: Up to 1 month after surgery

    Requirement for additional stone-related procedures

  10. Incremental Cost-Effectiveness Ratio Comparing 6.3Fr and 7.5Fr Mini-Flexible Ureteroscopes

    Time frame: From surgery through 30 days after surgery

    The incremental cost-effectiveness ratio (ICER) will compare the additional direct medical cost associated with the 6.3Fr versus 7.5Fr mini-flexible ureteroscope relative to the incremental clinical effectiveness. Direct medical costs will include ureteroscope acquisition costs, repair costs, procedure-related disposables, operating room time, hospital stay, management of complications, readmissions, and secondary procedures. Clinical effectiveness will be assessed primarily using stone-free and successful primary access outcomes.

Study contacts

Contact information is provided by the study sponsor or research team.

Asad O Naveed, MD

CONTACT

[email protected]

6478700880

Yasser A Noureldin, MD, PhD

CONTACT

[email protected]

416-318-2239

Sponsors and collaborators

Lead sponsor

Sault Area Hospital

Other

Registry information

Official study title

Outcomes and Cost-Effectiveness of 6.3French vs. 7.5French Mini-Flexible Ureteroscopy in the Treatment of Renal Stones: A Non-Inferiority, Prospective, Randomized, Single-Blinded Study

Acronym: MINI-FURS

Important dates

Study start
2026
Primary completion
2028
Study completion
2028
First posted
Sep 1, 2026
Registry last updated
Sep 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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