Changes of microRNA Expression in Obstructive and Neurogenic Bladder Dysfunction
NCT ID: NCT02410876
Last Updated: 2021-04-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
50 participants
OBSERVATIONAL
2015-06-30
2020-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Long-term Urodynamics in Individuals With Neurogenic Lower Urinary Tract Dysfunction
NCT02443870
Quality, Cost and Treatment Success on Patients With Lower Urinary Tract Dysfunction Undergoing Urodynamic Examination
NCT05809154
Health-related Quality of Life of Patients With Neurogenic Bladder
NCT02179073
An Exploratory Study to Investigate Bladder Contractions in the Storage Phase and Related Bladder Sensations in Healthy Females and Females With Overactive Bladder (OAB) Using High Resolution and Conventional Urodynamics
NCT01540786
Role of Residual Urine and Asymptomatic Prostatitis in the Development of Urinary Tract Infections in Spinal Cord Injury
NCT01601041
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
In a previous project, the investigators have established micro ribonucleic acid (miRNA) and messenger ribonucleic acid (mRNA) expression profiles of several urodynamically defined states of BLUTD. In this follow-up project, the investigators propose to extend these studies, undertaking a comparative miRNA and RNA profiling of BLUTD and NLUTD, and investigate the dynamic alteration of microRNA expression in different functional manifestations of disease. The investigators propose to validate primary gene targets of miRNAs differentially expressed in urodynamically defined states of BLUTD and identify signaling pathways, activated during the progression from hypertrophy to decompensation. Monitoring the reversal of changes in miRNA expression after relief of obstruction and restoration of normal bladder function will help delineate the key BOO-induced miRNAs with regulatory potential. Similarly, the dynamics of miRNA alteration, observed in SCI patients during the development and management of NLUTD should reveal the role of miRNA in gene expression regulation during neurogenic-induced organ remodelling.
By uncovering the molecular similarities and differences between BLUTD and NLUTD, the investigators will elucidate some of the causative factors in the development of these disorders and highlight the impact of myogenic and neurogenic components postulated to be involved. The project involves close collaboration between clinical and basic research, and combines the analysis of human biopsy material with in vitro cell-based assays, creating a comprehensive platform for the dissection of molecular mechanisms of LUTD. This project will keep the momentum of the investigators' previous research and contribute to the basic and applied studies into bladder remodeling. It is a logical continuation of their on-going studies of the role of miRNAs in LUT disorders but represents a novel direction of research and has high diagnostic and therapeutic potential.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Controls
No lower urinary tract symptoms undergoing cystoscopy in anesthesia for stone treatment or microhematuria assessment.
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Spinal cord injury/acontractile
Patients with traumatic spinal cord injury (SCI) with no (neither spontaneous nor provoked) detrusor activity during the filling phase of urodynamics.
Bladder biopsy 6 weeks after trauma 6 months later urodynamic study and bladder biopsy
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Urodynamic study
Assessment of bladder function through intravesical and intrabdominal pressure measurements according to International Continence Society standards.
Spinal cord injury/Detrusor overactivity
SCI patients with proven detrusor (urodynamics) overactivity during the filling phase.
Bladder biopsy 6 weeks after trauma 6 months later urodynamic study and bladder biopsy
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Urodynamic study
Assessment of bladder function through intravesical and intrabdominal pressure measurements according to International Continence Society standards.
Prostatic obstruction/acontractile
Low flow to no flow, no measurable detrusor activity on urodynamic evaluation, cystoscopy in line with obstruction.
Bladder biopsy at TURP (transurethral resection prostate) 3 months later urodynamic study and bladder biopsy
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Urodynamic study
Assessment of bladder function through intravesical and intrabdominal pressure measurements according to International Continence Society standards.
Prostatic obstruction/ obstructed
Obstruction according to Schäfer nomogram on urodynamic evaluation. Bladder biopsy at TURP 3 months later urodynamic study and bladder biopsy
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Urodynamic study
Assessment of bladder function through intravesical and intrabdominal pressure measurements according to International Continence Society standards.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Bladder biopsy
Small biopsy of the bladder is taken with cold-cup tongs.
Urodynamic study
Assessment of bladder function through intravesical and intrabdominal pressure measurements according to International Continence Society standards.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Planned TURP (transurethral prostate resection) (BLUTD)
* Spinal cord injury (in last 6 weeks) (NLUTD)
* Prior urodynamic study
* Informed consent
Exclusion Criteria
* Pregnancy
* Urinary tract infection
* History of or current genitourinary tuberculosis, bladder malignancy, radiotherapy.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Swiss National Science Foundation
OTHER
Balgrist University Hospital
OTHER
Insel Gruppe AG, University Hospital Bern
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Fiona C Burkhard, MD
Role: PRINCIPAL_INVESTIGATOR
Insel Gruppe AG, University Hospital Bern
Jürgen Pannek, MD
Role: PRINCIPAL_INVESTIGATOR
Swiss paraplegic center Nottwil
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University Hospital Inselspital
Bern, , Switzerland
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
331/2014
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.