Scientists hunt for clues in gut and urine to understand urinary blockages
NCT ID NCT07409870
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This observational study will compare the gut and urine bacteria, as well as metabolic profiles, of 120 people with ureteral stricture (a narrowing of the tube from kidney to bladder) against healthy volunteers. Researchers aim to find differences that could explain why the condition develops and identify potential markers for diagnosis. Participants provide stool, urine, and blood samples and undergo standard imaging and lab tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could identify new biomarkers for diagnosing or monitoring ureteral stricture, and point toward future microbiome-based treatments.
- What could go wrong
- This is an early observational study, not a treatment trial. It may not find clear differences, and any discoveries would need years of further research to become useful.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Feb 2026
An estimate. Start dates often move.
- Expected to finish
-
Jul 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population consists of adult patients diagnosed with ureteral stricture who are seeking medical consultation or surgical treatment at the Department of Urology in a tertiary medical center The First Affiliated Hospital of Chongqing Medical University. These patients represent a diverse range of etiologies, including iatrogenic, inflammatory, and idiopathic narrowing. Simultaneously, a cohort of healthy volunteers will be recruited from the hospital's physical examination center or the local community to serve as the control group. These volunteers are age- and sex-matched to the patient group and share a similar geographic and dietary background to minimize environmental confounding factors in microbiome and metabolomic analysis.
- Ages
-
Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria (Ureteral Stricture Group): Age between 18 and 75 years, regardless of gender. Diagnosis of ureteral stricture confirmed by clinical symptoms and imaging (e.g., CT, IVP, or retrograde pyelography) or ureteroscopy. The patient is scheduled for or undergoing standard clinical evaluation/treatment for ureteral stricture. Willingness to provide stool, urine, and blood samples. Informed consent signed by the participant or their legal representative. Inclusion Criteria (Healthy Control Group): Age- and sex-matched volunteers (18-75 years). No history of ureteral stricture, urinary tract obstruction, or significant renal disease. Physical examination and laboratory tests (renal function, routine urine analysis) are within normal limits. Exclusion Criteria (Applicable to Both Groups): Use of antibiotics, probiotics, prebiotics, or antifungal medications within the 4 weeks prior to sample collection. History of chronic gastrointestinal diseases (e.g., Inflammatory Bowel Disease (IBD), Irritable Bowel Syndrome (IBS), or chronic diarrhea). Known malignant tumors of the urinary tract or other systemic malignancies. History of major abdominal or urinary tract surgery within the last 3 months (excluding the current planned procedure for patients). Presence of severe systemic diseases, including uncontrolled diabetes, severe hepatic dysfunction, or end-stage heart failure. Pregnancy or breastfeeding. Any other condition that, in the opinion of the investigator, may interfere with the microbiome or metabolomic analysis.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Metabolomics are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Department of Urology, The First Affiliated Hospital of Chongqing Medical University
Chongqing, 400016, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Fish oil meets TB drugs: can Omega-3 help clear infection faster?
- Can a stronger flu shot boost immunity in older adults?
- Can pond scum become a protein powerhouse? a trial tests microalgae drinks
- Switching stomach drugs after transplant may tame a deadly immune attack
- Can a fiber supplement reshape the small Intestine's hidden microbiome?
- Could a simple fibre supplement reshape your gut microbiome?