Study of the Spermatic Characteristics of Patients With Fabry Disease (FERTIFABRY)
Primary Purpose
Fabry Disease
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Semen collection
Sponsored by
About this trial
This is an interventional diagnostic trial for Fabry Disease
Eligibility Criteria
Inclusion Criteria:
- male patients with Fabry disease regardless of the clinical form of the disease; treated with enzyme replacement therapy or not (from the initial diagnosis). The definite diagnosis of Fabry disease will be established on the deficit of the activity of alpha galactosidase A (<12%). A molecular genetic study is desirable but not mandatory,
- patients aged 18 to 65,
- giving their free and informed consent to participate, after information on the research.
Exclusion Criteria:
- persons placed under the protection of justice,
- unaffiliated or non-beneficiary subject of a social security scheme.
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Single arm
Arm Description
Men with Fabry Disease
Outcomes
Primary Outcome Measures
volume (ml) of sperm
Spermogram characteristics
pH of sperm
Spermogram characteristics
Count (million / ml) of spermatozoids
Spermogram characteristics
Mobility (%) and mobility type of spermatozoa according to WHO classification of spermatozoids
Spermogram characteristics
Total number of spermatozoa in one ejaculate
Spermogram characteristics
Total number of progressive motile spermatozoa
Spermogram characteristics
Existence of leukospermia yes/no
Spermogram characteristics
% of typical forms of spermatozoids
Characteristics of spermocytogram
Multiple Anomalies Index (MAI) of spermatozoids
Characteristics of spermocytogram
Secondary Outcome Measures
Full Information
NCT ID
NCT04073888
First Posted
August 23, 2019
Last Updated
August 27, 2019
Sponsor
University Hospital, Bordeaux
1. Study Identification
Unique Protocol Identification Number
NCT04073888
Brief Title
Study of the Spermatic Characteristics of Patients With Fabry Disease
Acronym
FERTIFABRY
Official Title
Study of the Spermatic Characteristics of Patients With Fabry Disease
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
February 20, 2009 (Actual)
Primary Completion Date
October 18, 2013 (Actual)
Study Completion Date
October 18, 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objective of this project is to estimate the prevalence of spermatic abnormalities in patients with Fabry disease.The main objective of this project is to estimate the prevalence of spermatic abnormalities in patients with Fabry disease.
Detailed Description
Fabry disease is a lysosomal storage burden of X-linked genetic transmission due to alpha-galactosidase deficiency. This enzyme deficiency causes deposits of globotriaosylceramide in virtually all cell types of the body. The majority of hemizygous men develop a severe multisystemic disease dominated by renal failure, neurological and cardiac involvement. There is a specific treatment based on enzyme replacement therapy.
The incidence of Fabry disease is estimated between 1/60000 and 1/3500 in the general population.
Infertility in Fabry disease is poorly documented. Only a few cases have been reported, from alteration of spermogram to azoospermia. The identification of deposits suggestive of Gb3 in light microscopy and electron microscopy at the level of the genital tract argues in favor of the attack of this device. The low prevalence of Fabry disease requires a cross-sectional multicenter study to determine the frequency of alterations in sperm characteristics, their impact on fertility, and the possible effect of substitution therapy, in order to establish appropriate measures. adequate preventive measures.
The objective of this project is to estimate the prevalence of spermatic abnormalities in patients with Fabry disease.The main objective of this project is to estimate the prevalence of spermatic abnormalities in patients with Fabry disease.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fabry Disease
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Single arm
Arm Type
Other
Arm Description
Men with Fabry Disease
Intervention Type
Procedure
Intervention Name(s)
Semen collection
Intervention Description
Semen collection for seminogram and spermocytogram
Primary Outcome Measure Information:
Title
volume (ml) of sperm
Description
Spermogram characteristics
Time Frame
At Day 1
Title
pH of sperm
Description
Spermogram characteristics
Time Frame
At Day 1
Title
Count (million / ml) of spermatozoids
Description
Spermogram characteristics
Time Frame
At Day 1
Title
Mobility (%) and mobility type of spermatozoa according to WHO classification of spermatozoids
Description
Spermogram characteristics
Time Frame
At Day 1
Title
Total number of spermatozoa in one ejaculate
Description
Spermogram characteristics
Time Frame
At Day 1
Title
Total number of progressive motile spermatozoa
Description
Spermogram characteristics
Time Frame
At Day 1
Title
Existence of leukospermia yes/no
Description
Spermogram characteristics
Time Frame
At Day 1
Title
% of typical forms of spermatozoids
Description
Characteristics of spermocytogram
Time Frame
At Day 1
Title
Multiple Anomalies Index (MAI) of spermatozoids
Description
Characteristics of spermocytogram
Time Frame
At Day 1
10. Eligibility
Sex
Male
Gender Based
Yes
Gender Eligibility Description
Semen collection
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
male patients with Fabry disease regardless of the clinical form of the disease; treated with enzyme replacement therapy or not (from the initial diagnosis). The definite diagnosis of Fabry disease will be established on the deficit of the activity of alpha galactosidase A (<12%). A molecular genetic study is desirable but not mandatory,
patients aged 18 to 65,
giving their free and informed consent to participate, after information on the research.
Exclusion Criteria:
persons placed under the protection of justice,
unaffiliated or non-beneficiary subject of a social security scheme.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alice PAPAXANTHOS, Dr
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Study of the Spermatic Characteristics of Patients With Fabry Disease
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