- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02144558
Fertility of Spinal Cord Injured Men (FertiSCI)
Evolution of Sperm Parameters and Study of Risk Factors of Impairment of Sperm Quality in Spinal Cord Injuries. Longitudinal Prospective Study.
Spinal cord injured (SCI) men, para or tetraplegic, most often have an infertility, caused among others by a deficiency of sperm quality particularly motility and vitality. Several mechanisms have been proposed: low frequency of ejaculation, recurrent urinary tract and seminal infections, presence of an inflammatory syndrome (IS) and an oxidative stress (OS). However, no French study of sperm quality has been conducted in this population that could identify aggravating factors of sperm quality and a way to prevent them.
Hypothesis: Sperm parameters decrease rapidly following spinal cord injury and next stabilise. However, unidentified yet risk factors could influence long-term evolution of sperm parameters.
The objective is to study the evolution of sperm parameters during 18 months taking into account bladder management, recurrent urinary tract and bladder infections, IS and OS. The evaluation of these parameters and their consequences will be indicative to determine one or more risk factors of sperm degradation and determine a strategy for long term support to avoid the use of ART either by sperm cryopreservation and/or by preventing risk factors
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
SCI men are mostly young adults who have not completed their parental project. Infertility has many causes: erectile dysfunction, anejaculation (85% of SCI ) and altered sperm parameters. Penile vibratory stimulation allows 75 % of the sperm collection. If sperm quality is sufficient, intravaginal insemination of their partner at home is possible. The use of AMP remains common, which is damaging to men non sterile priori. In SCI, sperm concentration remains satisfactory but mobility and vitality are impaired. The installation of this irreversible degradation likely occurs very quickly after the trauma. The possible deterioration of sperm parameters with time is not known. The following pathophysiological mechanisms have been proposed: i) increased scrotal temperature, ii) decreased ejaculatory frequency, iii) recurrent urinary tract and seminal infections, iv ) inflammation and oxidative stress in the semen. Patients, and even rehabilitation doctors often submit an application for preventive sperm conservation but in the absence of prospective longitudinal data on the evolution of sperm quality of SCI men over the time and identified risk factors of degradation, the indication and timing of preventive cryopreservation remain to be defined.
Hypothesis: The sperm parameters, mobility and vitality, in SCI patients with or without penile vibratory stimulation (PVS), decrease in the immediate aftermath of trauma and next stabilize out the occurrence of intercurrent medical events or symptomatic urogenital infections. However, unidentified yet risk factors could influence long-term evolution of these sperm parameters.
Main objective: Monitoring the evolution of sperm parameters for 18 months: concentration, mobility, vitality, sperm morphology, inflammatory syndrome and oxidative stress on 4 ejaculates collected by masturbation or SVP at 6-month intervals.
Secondary objectives: In case of impaired sperm quality, identify risk factors for this change.
SCI men will have 4 medical visits associated to sperm retrieval spaced to 6 months during 18 months. At each visit medical and reproductive informations will be collected.
Knowledge of the evolution of sperm parameters and risk factors of its degradation over time must answer with the criteria of "evidence based medicine" the request of sperm cryopreservation frequently expressed by SCI patients. This study should lead to the optimization of the management of infertility in patients with spinal cord injuries and giving directions for research aiming to prevent the degradation of sperm parameters. Finally, this study should provide the rationale for future research on clinical risk factors and / or biological degradation of sperm and biological markers of risk of degradation.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Paris, France, 75014
- Assistance Publique-Hôpitaux de Paris, Cochin Hospital, Department of Biology of Reproduction
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Spinal cord injured men aged between 18 and 60 years
- Strict antegrade ejaculation obtained by masturbation or penil vibratory stimulation
- Signature of an informed and written consent to participate to the study.
Exclusion Criteria:
- Total or partial retrograde ejaculation
- Major patients protected
- Men no affiliated with a french social security regime.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Spinal cord injured (SCI) men, para or tetraplegic
SCI men will have 4 medical visits associated to sperm retrieval (penile vibratory stimulation (PVS) or masturbation)
|
penile vibratory stimulation (PVS) or masturbation
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Time Frame: 18 month
|
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart. |
18 month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
spermogram
Time Frame: 18 months
|
Sperm concentration, mobility and morphology
|
18 months
|
elastase
Time Frame: 6 month
|
Measure of inflammation
|
6 month
|
DNA fragmentation
Time Frame: 18 months
|
Sperm DNA integrity, measures oxidative stress
|
18 months
|
8 Hydroxydesoxyguanosine (8OHdG)
Time Frame: 18 months
|
Oxydative stress
|
18 months
|
Seminal biochemistry
Time Frame: 18 months
|
Secretion of seminal tract
|
18 months
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Urinary and seminal infections
Time Frame: 18 months
|
Bacteriological analysis of sperm and urine
|
18 months
|
Mode of urinary catheter
Time Frame: 18 months
|
18 months
|
|
Spinal cord injury type
Time Frame: 0 months
|
Type and level of the lesion
|
0 months
|
Concomitant treatments
Time Frame: 18 months
|
18 months
|
|
Patient age and time to spinal cord injury
Time Frame: 18 months
|
18 months
|
|
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Time Frame: 6 months
|
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart. |
6 months
|
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Time Frame: 12 months
|
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart. |
12 months
|
Sperm viability: percent of live spermatozoa among 100 counted spermatozoa.
Time Frame: 0 months
|
Sperm viability is a stable criteria of evaluation and it has a good repeatability in our lab. Sperm viability is measured on fresh sperm 30 minutes after ejaculation using eosine nigrosine coloration. This measure is repeated on each of the four ejaculates obtained at 6 months apart. |
0 months
|
elastase
Time Frame: 0 month
|
Measure of inflammation
|
0 month
|
elastase
Time Frame: 12 month
|
Measure of inflammation
|
12 month
|
elastase
Time Frame: 18 month
|
Measure of inflammation
|
18 month
|
spermogram
Time Frame: 0 months
|
Sperm concentration, mobility and morphology
|
0 months
|
spermogram
Time Frame: 6 months
|
Sperm concentration, mobility and morphology
|
6 months
|
spermogram
Time Frame: 12 months
|
Sperm concentration, mobility and morphology
|
12 months
|
DNA fragmentation
Time Frame: 0 month
|
Sperm DNA integrity, measures oxidative stress
|
0 month
|
DNA fragmentation
Time Frame: 6 months
|
Sperm DNA integrity, measures oxidative stress
|
6 months
|
DNA fragmentation
Time Frame: 12 months
|
Sperm DNA integrity, measures oxidative stress
|
12 months
|
8 Hydroxydesoxyguanosine (8OHdG)
Time Frame: 0 months
|
Oxydative stress
|
0 months
|
8 Hydroxydesoxyguanosine (8OHdG)
Time Frame: 6 months
|
Oxydative stress
|
6 months
|
Seminal biochemistry
Time Frame: 0 months
|
Secretion of seminal tract
|
0 months
|
Seminal biochemistry
Time Frame: 6 months
|
Secretion of seminal tract
|
6 months
|
Seminal biochemistry
Time Frame: 12 months
|
Secretion of seminal tract
|
12 months
|
Urinary and seminal infections
Time Frame: 0 months
|
Bacteriological analysis of sperm and urine
|
0 months
|
Urinary and seminal infections
Time Frame: 6 months
|
Bacteriological analysis of sperm and urine
|
6 months
|
Urinary and seminal infections
Time Frame: 12 months
|
Bacteriological analysis of sperm and urine
|
12 months
|
Mode of urinary catheter
Time Frame: 0 months
|
0 months
|
|
Mode of urinary catheter
Time Frame: 6 months
|
6 months
|
|
Mode of urinary catheter
Time Frame: 12 months
|
12 months
|
|
Concomitant treatments
Time Frame: 0 month
|
0 month
|
|
Concomitant treatments
Time Frame: 6 months
|
6 months
|
|
Concomitant treatments
Time Frame: 12 months
|
12 months
|
|
Patient age and time to spinal cord injury
Time Frame: 0 month
|
0 month
|
|
Patient age and time to spinal cord injury
Time Frame: 6 months
|
6 months
|
|
Patient age and time to spinal cord injury
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Céline Chalas, PhD, Cochin Hospital
Publications and helpful links
General Publications
- Iremashvili V, Brackett NL, Ibrahim E, Aballa TC, Lynne CM. Semen quality remains stable during the chronic phase of spinal cord injury: a longitudinal study. J Urol. 2010 Nov;184(5):2073-7. doi: 10.1016/j.juro.2010.06.112. Epub 2010 Sep 17.
- Padron OF, Brackett NL, Sharma RK, Lynne CM, Thomas AJ Jr, Agarwal A. Seminal reactive oxygen species and sperm motility and morphology in men with spinal cord injury. Fertil Steril. 1997 Jun;67(6):1115-20. doi: 10.1016/s0015-0282(97)81448-3.
- Brackett NL, Ibrahim E, Grotas JA, Aballa TC, Lynne CM. Higher sperm DNA damage in semen from men with spinal cord injuries compared with controls. J Androl. 2008 Jan-Feb;29(1):93-9; discussion 100-1. doi: 10.2164/jandrol.107.003574. Epub 2007 Sep 5.
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 (Estimate)
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
- P130703
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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