- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03189056
Lower Urinary Tract Dysfunction in Chronic Chagas' Disease : Clinical and Urodynamic Presentation
Chagas disease is one of the most neglected vector-borne infectious disease worldwide. The first decades following the discovery of the pathology drove an international research enthusiasm, mainly concentrated on understanding the typical cardiac and digestive forms. Recently, research have been focused on vector control, which has been a huge success, at the price of neglecting the patients who already presented fixed and severe organic lesions due the chronic phase of the illness.
This study focus on a rarely studied aspect of this pathology: the involvement of the lower urinary tract and it's symptomatology in adults suffering from Chagas chronic disease.
Various studies have assessed the involvement of the lower urinary tract in chronic Chagas disease, the vast majority of them being on the animal model or very ancient human studies mainly on cadaveric specimen, the first of them being the primary description of Koeberle in 1963.
Human symptomatology deriving from bladder, ureteral and urethral chronic chagasic lesions are yet widely unknown, and only a few Brazilian and Mexican studies have intended to describe the clinical and urodynamic presentation of these patients.
The aim of this study is to assess the prevalence of urinary disorders in chronic chagasic patients and to describe their symptoms, through a complete clinical, ultrasonographic and urodynamic description.
Study Overview
Status
Intervention / Treatment
Detailed Description
Epidemiologic observationnal transversal study
Cohort of patients between 18 and 50 years of age, presenting a chronic form of Chagas' disease (cardiopathy, mega-colon or mega-esofagus), and presenting non of the exclusion criteria.
Recruitment via the existing patients list of positive Chagas serology of:
- the SELADIS center (Instituto de Servicios de Laboratorio de Diagnostico e Investigacion en Salud UMSA -UNIVERSIDAD MAYOR DE SAN ANDRES-)
- Private surrounding hospitals, Hospital de Clinicas and Centro de Seguro Social Universitario de La Paz (UMSA)
- Laboratorio de Inmunodiagnostico Instituto Boliviano de Biologia de la Altura -IBBA-Dr Lourdes Echalar.
Informed consent signed.
1 to 3 consultations on a period of one to 2 weeks no follow-up (transversal study)
Invasive descriptive explorations (blood sample and urodynamic study, imposing the assent of the Comité Nacional de Bioética).
Main objective : Describe the prevalence of the lower urinary tract dysfunction in patients suffering from a chronic form of Chagas' disease. The main criteria evaluated is the sum of two symptom questionnaires IPSS and ICIQ (spanish official validated translation), focusing on urinary incontinence, voiding dysfunction and quality of life.
Secondary objectives :
All the included patients will be proposed an initial consult :
- Anonymization of all the observation/results
- Past history (pathology, actual treatment,…), search of the exclusion criteria, Chagas' disease symptomatology and treatment, urological symptomatology.
- Validated questionnaires to evaluate urological symptoms, urinary incontinence, voiding dysfunction or acute urinary dysfunction, bladder hyperactivity, sexuality and fertility.
- Clinical examination
- Micturition calendar /48hours.
- Uroflowmetry, followed by ultrasonography for post-void residual and upper-urinary tract dilatation.
- Blood sample to evaluate renal function (plasmatic creatinina for CDK EPI formula). This blood sample can also be used to confirm the positive Chagas' serology if no serology is available (indirect immunofluorescence and ELISA).
Te participants presenting a symptomatic lower urinary tract dysfunction on the previous exams will be proposed a complete urodynamic exploration (cystomanometry, urethral profile, pression/flow study during mycturition).
Sterility of urine assessed before exam. Tecnical material imported from Spain, Albyn medical Smardyn and consummables. Electronic curves obtained from Phoenix software (Albyn).
Objective inclusion of 200 participants during 5 months, between June and October 2017, in the SELADIS Institute in La Paz, Bolivia. Director of study Dr Simone Frédérique Brenière (french), Bolivian Director of Institute Dra Susana Revollo.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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La Paz, Bolivia
- SELADIS Institute, Universidad Mayor de San Andrès
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Male or female between 18 and 50 years of age
- Presenting a chronic form of Chagas disease : cardiopathy or enteropathy
- Previously treated or not treated
- Signed informed consent
Exclusion Criteria:
- Diabetes
- Neurologic pathology
- Past history of extensive pelvic surgery
- Vaginal prolaps > grade 3 of Baden & Walker (female)
- Past history of vertebral fracture > L2
Study Plan
How is the study designed?
Design Details
- Observational Models: Ecologic or Community
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Single cohort
single cohort for transversal study patients presenting chronic chagas disease for all patients : clinical examination/questionnaires/ quality of life/ blood sample for renal function (creatinina) and Chagas serology control if needed/ uroflowmetry/ ultrasonography If symptomatic patient at first exploration : urodynamic exploration is proposed (cystomanometry, urethral profile, pressure/flow study). No electromyograma. No video urodynamic procedure. |
IFI + ELISA method if no biological confirmation of chagas disease is in our possession
Plasmatic single mesure after consultation 1, to evaluate renal function
With a new equipement SmartDyn Albynmedical imported from Spain for the study Single use sterile equipment shipped Control of urine sterility before procedure Informed consent signed If acquired urinary infection after procedure, patient treated free of charge and clinical evolution controlled
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Symptomatic patients
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
|
ICIQ SF>0 IPSS>7 or past acute urinary retention IIEF5<11
|
at consultation : 1 day (transversal study, the participant will not be followed)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Megabladder
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
|
Bladder capacity >600cc and <4 daily micturition
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at consultation : 1 day (transversal study, the participant will not be followed)
|
Mega ureter
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
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Ultrasonographic dilatation of renal pelvis>20mm or of ureter >7mm
|
at consultation : 1 day (transversal study, the participant will not be followed)
|
Hyperactive bladder
Time Frame: micturition calendar over 2 days (transversal study, the participant will not be followed)
|
>8 daily micturition + urgency on dairy subsection detrusor hyperactivity on cystomanometry
|
micturition calendar over 2 days (transversal study, the participant will not be followed)
|
Detrusor underactivity
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
|
Qmax<15 mL/s and post void residual>150cc per-micturition pressure <40 cm H2O
|
at consultation : 1 day (transversal study, the participant will not be followed)
|
Renal insufficiency
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
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CDK EPI<60 mL/mn
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at consultation : 1 day (transversal study, the participant will not be followed)
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Urinary recurrent infections
Time Frame: reported infections duing the last 5 years (transversal study, the participant will not be followed)
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past history > 3 pyélonephritis or >5 cystitis/year in the past 5 years, if associated with dilatated ureter/renal pelvis or significant post void residual
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reported infections duing the last 5 years (transversal study, the participant will not be followed)
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Urinary sphincter insufficiency
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
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P max<30 cm H20 and stress urinary incontinence
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at consultation : 1 day (transversal study, the participant will not be followed)
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Erectile dysfunction in males
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
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IIEF5 <16
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at consultation : 1 day (transversal study, the participant will not be followed)
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Hypofertility
Time Frame: at consultation : 1 day (transversal study, the participant will not be followed)
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oral assess by difficulty to obtain pregnancy >1 year
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at consultation : 1 day (transversal study, the participant will not be followed)
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Elsa BEY, Resident, IRD
Publications and helpful links
Helpful Links
- Jelicks, Linda A., et Herbert B. Tanowitz. " Advances in Imaging of Animal Models of Chagas Disease ". Advances in Parasitology 75 (2011): 193-208. doi:10.1016/B978-0-12-385863-4.00009-5.
- Ny, Lars et al. " A Magnetic Resonance Imaging Study of Intestinal Dilation in Trypanosoma Cruzi-Infected Mice Deficient in Nitric Oxide Synthase ". The American Jour
- Barr et al. " Canine Chagas' Disease (American Trypanosomiasis) in North America ". Veterinary Clinics of North America: Small Animal Practice, Small Animal Parasites: Biology and Control, 39, nᵒ 6 (novembre 2009): 1055-64. doi:10.1016/j.cvsm.2009.06
- Ardito et al. " Chronic Renal Impairment in Patients with Chagas Cardiomyopathy with Chronic Systolic Heart Failure: Prevalence and Prognostic Significance ". Inte
- Koeberle, F. " ENTEROMEGALY AND CARDIOMEGALY IN CHAGAS DISEASE ". Gut 4 (décembre 1963): 399-405.
- Mirkin et al. " Experimental Chagas' Disease: Electrophysiology and Cell Composition of the Neuromyopathic Inflammatory Lesions in Mice Infected with a Myotropic and a Pantropic Strain of
- Cabrine-Santos et al. " Genitourinary Changes in Hamsters Infected and Reinfected with Trypanosoma Cruzi ". Memórias Do Insti
- Scremin, L. H., C. E. Corbett, M. D. Laurenti, E. V. Nunes, J. J. Gama-Rodrigues, et M. Okumura. " Megabladder in Experimental Chagas Disease: Pathological Features of the Bladder Wall ". Revista Do Hospital Das Clínicas 54, nᵒ 2 (avril 1999): 43-46.
- Suaid et al. " Modulation of Urethral Alpha-Sympathetic by Parasympathetic before and Following Bethanechol Chloride Injection ". International Braz J Urol: Official J
- Said, G�rard, Mireille Joskowicz, Amilton Antunes Barreira, et Harvey Eisen. " Neuropathy Associated with Experimental Chagas' Disease ". Annals of Neurology 18, nᵒ 6 (décembre 1985): 676-83. doi:10.1002/ana.410180609.
- DeFaria, C. R., J. M. De Rezende, et A. Rassi. " [Peripheral denervation in the various clinical forms of Chagas' disease] ". Arquivos De Neuro-Psiquiatria 46, nᵒ 3 (septembre 1988): 225-37.
- Scremin et al. " T.cruzi induces megabladder in experimental chagas disease ". Parasitology International 47, Supplement 1 (août 1998): 200. doi:10.1016/S1383-5769(98)80520-5.
- Carraro, A. A., R. A. Lopes, R. D. Ribeiro, et T. L. Lamano Carvalho. " The Male Reproductive Organs in the Chronic Phase of Experimental Chagas' Disease ". Angewandte Parasitologie 33, nᵒ 1 (février 1992): 3-9.
- Boczko et al. " Trypanosoma Cruzi Infection Induced Changes in the Innervation, Structure and Function of the Murine Bladder ". The Journal of Urology 173, n
- Rocha, J. N., H. J. Suaid, A. C. P. Martins, A. J. Cologna, S. Tucci Jr., et M. A. Gonçalves. " URODYNAMIC ASSESSEMENT IN PATIENTS WITH CHAGAS DISEASE ". Acta Cirurgica Brasileira 16 (2001): 7-8. doi:10.1590/S0102-86502001000500003.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Chagas_urology
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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