Kansas City, KSNCT07071831Now EnrollingIRB Ready

Renal Stones Clinical Trial in Kansas City, KS

Access cutting-edge renal stones treatment through this clinical trial at a research site in Kansas City. Study-provided care at no cost to qualified participants.

Sponsored by University of Kansas Medical Center

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Expert Care in Kansas City

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IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related renal stones treatment provided free

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Check if you qualify for this renal stones clinical trial in Kansas City, KS

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Why Participate?

  • No-Cost Study Care

  • Local to Kansas City

    Convenient for KS residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Kansas City site if eligible
  4. 4Begin participation

About This Renal Stones Study in Kansas City

The goal of this observational study is to learn about the benefit of using RetroPerc® in obtaining renal access for percutaneous nephrolithotomy. The device is already used in routine clinical practice by urologists around the country. Participants who are already scheduled to undergo percutaneous nephrolithotomy as part of their regular care will be asked to participate.

Sponsor: University of Kansas Medical Center

Who Can Participate

Inclusion Criteria

Renal stone or total linear sum of 1.5-3cm cm in maximum dimension (largest diameter in axial or coronal)--- multiple stones should be summed to determine stone size.
Age \>=18 years of age
Gender: both men and women included.
Ethnic background: all ethnicities will be included in the study population and the specific ethnic diversity present in the study population will reflect the geographic distributions of the participating institutions.
Plan for PCNL in the supine position

Exclusion Criteria

Active pregnancy
Severe Hydronephrosis - renal pelvis diameter \> 20mm
Flank window \< 4 cm are ineligible for puncture
Previous ipsilateral PCNL
Currently with "useful" nephrostomy tube on ipsilateral side
Uncorrectable coagulopathies
Untreated urinary tract infection
Subjects with significant morbidities such as American Society of Anesthesiologists (ASA) score ≥ 4, severe spinal cord injuries, severe cardiopulmonary insufficiency, uncontrolled diabetes, neurological disorders, bedbound, anticipated life expectancy less than 5 years, or any other comorbidity, that in the opinion of the principal investigator could represent an increased peri-operative risk for the subject;
Ipsilateral partial nephrectomy
History of ipsilateral ureteral reimplantation or ureteral reconstruction;
History of Simple or radical prostatectomy
History of cystectomy
History of calyceal diverticula stone;
History of renal donation or transplant;
Any other previous pelvic surgical treatment that could put the subject at greater procedural complication risk or technical difficulty;
Ureteral ipsilateral stricture, untreated;
Ureteral stricture, untreated (not to include "tight" ureter);
Any other bladder, ureteral or kidney congenital genitourinary abnormalities (e.g. Horseshoe kidney, ipsilateral duplicated or partially duplicated collecting system, ipsilateral ectopic kidney, cross-fused ectopia, bifid renal pelvis with no horizontally directed calyces, solitary kidney, etc.) preventing the ability to direct a puncture laterally or render the subject stone free;
Have participated in any other clinical trial within the last 3 months, and/or plans to participate in any other investigational or invasive clinical trial during this study;
If female, breast-feeding, or if childbearing age, is not using contraception between screening and 90 days post-op;
Subject has current or recent history of substance abuse (e.g. recreational drugs, narcotics, or alcohol) requiring intervention;
Is a prisoner or ward of the state;
Is unable to meet the treatment and follow up protocol requirements.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Kansas City?

Yes, this clinical trial (NCT07071831) has an active research site in Kansas City, KS that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Renal Stones Treatment Options in Kansas City, KS

If you're searching for renal stones treatment options in Kansas City, KS, this clinical trial (NCT07071831) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Kansas City research site is actively enrolling participants for this clinical trial. You'll receive care from experienced renal stones specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all renal stones clinical trials near you to find additional studies recruiting in your area.

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