- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03726450
Myo-inositol and an Antioxidant Mix for the Treatment of Vietnamese Infertile Men
December 11, 2019 updated by: Hung Nguyen Ba, Andrology and Fertility Hospital of Hanoi
Can Myo-inositol in Combination With N-Acetyl-Cysteine Plus an Antioxidant Mix be Useful for the Management of Men Affected by Idiopathic Infertility and Semen Hyperviscosity?
The aim of this study is to evaluate if Myo-inositol, N-Acetyl-Cysteine plus a cocktail of antioxidants could be able to increase spermatozoa parameters and reduce semen hyper-viscosity
Study Overview
Status
Unknown
Conditions
Detailed Description
According to the World Health Organization (WHO), the incidence of infertile couples is relatively high, with a range from 15% to 20% in the developed countries.
In accordance with WHO, spermatogenesis disorders occur in almost 50% of all the cases of male infertility.
In the recent decades, an unexplained reduction has been found, not only in sperm quality and quantity but also in the volume of the ejaculate.
This evidence allows speculations on the number of male infertility factors, which will keep increasing in the future.
An important impact on male infertility caused by environmental factors, such as bad habits (alcohol and smoking), body overload and in particular the reluctance of men undergoing prevention is widely reported.
A reduced fertility is often related to a lower sperm motility.
Over the recent years, the percentage of motile sperms in the ejaculate is constantly reducing.
For these reasons, WHO, in the latest edition, indicated a percentage of sperms progressive motility less than 32% as a parameter of the reduced chance of getting pregnant spontaneously.
The etiopathogenesis of male infertility is extremely complex, and the factors and processes causing these disorders in the reproduction are different.
A common cause of reduced sperms motility seems to be related to the toxic action of reactive oxygen species (ROS).
Pathological effects of free radicals in the male reproductive tract are associated with DNA fragmentation, lipid peroxidation, and apoptosis, and these lead to reduced fertility and miscarriages.
Due to this evidence, antioxidant species were introduced in the management of male infertility.
Between these molecules, Selenium and L-Arginine had shown a strong impact in contrasting ROS generation and restoring the oxidative status of the seminal environment.
Myo-inositol (MI) is an isomer of the inositol's family.
In nature are present 9 isomers of this sugar-like and MI represents the most abundant one.
It plays a key role in more than one cellular pathways as FSH, insulin and TSH second intracellular messenger.
It has been also demonstrated an important effect of MI in improving semen parameters such as motility, morphology, and quality, both in vitro and in vivo.
From the reported studies, the effect of this isomer seems to be related to an improvement in the membrane potential of spermatozoa's mitochondria and in the reduction of the semen amorphous material that frequently impairs male fertility.
Based on this evidence, recent scientific researches have been focused on the clinical use of MI in the management of male infertility caused by semen alterations.
A further growing issue impairing male fertility is semen hyperviscosity (SHV).
SHV is a condition that can seriously impair the physical and chemical characteristics of the seminal fluid and it can have a serious impact on sperm function.
Worth of spreading, SHV seems to be associated with reduced sperm motility, possibly due to a 'trapping effect' that prevents normal sperm progression through the female genital tract.
N-acetyl-L-cysteine (NAC) is a derivative of the naturally occurring amino acid L-cysteine that has free radical scavenging activity and it is also commonly used as a mucolytic agent.
In addition to NAC antioxidant activity, Cifci et al. found it effective in reducing semen viscosity and its oxidative status as well as in increasing semen volume and spermatozoa motility.
Study Type
Interventional
Enrollment (Anticipated)
55
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Hanoi, Vietnam
- Recruiting
- Hung Nguyen
-
Contact:
- Hung three Nguyen, Medical doctor
- Phone Number: +84 989 200 940
- Email: hung2779@gmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 55 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- BMI < 29
- One year of unsuccessful sexual intercourses without achieving pregnancy for male factor (idiopathic infertility)
- Normospermia, isolated asthenozoospermia and/or oligoasthenozoospermia
- Semen hyper-viscosity defined as severe, moderate and mild
Exclusion Criteria:
- The absence of spermatozoa production
- Positive presence of leucocyte and inflammation factor in the seminal fluid
- Positive urea test for the presence of bacteria, protozoa and/or fungi infection
- Diagnosis of cryptorchidism
- Diagnosis of Varicocele of grade 2 or higher
- Diagnosis of Diabetes and other pathology causing oxidative stress
- Concentration alterations of the following hormones: LH, FSH, Testosterone, Prolactin, 17b-estradiol
- Abuse of alcohol and controlled substance
- Smoking cigarettes (>10 cigarettes/day)
- BMI > 30
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Andrositol Plus
all the patients will be treated for three months with a dietary supplement containing Myo-inositol, NAC, Folic acid, selenium, vitamin E, L-Arginine and L-Carnitine
|
Myo-inositol
N-Acetyl-Cysteine
Folic Acid
Selenium
L-arginine
L-carnitine
Vitamin E
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in sperm motility
Time Frame: spermatozoa motility will be analyzed after 3 months of treatment
|
spermatozoa motility will be evaluated through microscopical evalutation
|
spermatozoa motility will be analyzed after 3 months of treatment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
change in sperm morphology
Time Frame: spermatozoa morphology will be analyzed at the enrollment and after 3 months of treatmentanalyzed
|
spermatozoa morphology will be evaluated through microscopical evalutation
|
spermatozoa morphology will be analyzed at the enrollment and after 3 months of treatmentanalyzed
|
|
change in sperm vitality
Time Frame: spermatozoa vitality will be analyzed after 3 months of treatment
|
spermatozoa vitality will be evaluated through vitality test with methylene blue
|
spermatozoa vitality will be analyzed after 3 months of treatment
|
|
change in sperm count
Time Frame: spermatozoa count will be 3 months of treatment
|
spermatozoa count will be evaluated through microscopical evalutation
|
spermatozoa count will be 3 months of treatment
|
|
change in seminal fluid viscosity
Time Frame: semen Hyper-viscosity will be analyzed after 3 months of treatment
|
Viscosity will be determined after ejaculation by gently aspirating semen into a 5 ml pipette and then producing semen drops.
|
semen Hyper-viscosity will be analyzed after 3 months of treatment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2018
Primary Completion (Anticipated)
February 1, 2020
Study Completion (Anticipated)
March 1, 2020
Study Registration Dates
First Submitted
September 7, 2018
First Submitted That Met QC Criteria
October 30, 2018
First Posted (Actual)
October 31, 2018
Study Record Updates
Last Update Posted (Actual)
December 12, 2019
Last Update Submitted That Met QC Criteria
December 11, 2019
Last Verified
March 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MAVIM
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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