Infertility, Male Clinical Trial
Official title:
A Double-blind Randomized Placebo-controlled Clinical Study to Verify the Efficacy of TetraSOD® in the Improvement of Semen Quality in Patients With Idiopathic Infertility
TetraSOD® is a unique marine phytoplankton (Tetraselmis chuii) SOD-rich ingredient that is grown under patent-protected technology exclusively designed by the company Fitoplancton Marino, S.L. (Spain). In a previous pilot trial, the ability of TetraSOD® to improve semen characteristics in idiopathic infertile men after three months of treatment was assessed, revealing significant improvements in almost all of the analyzed parameters. In the present clinical trial, such positive effects will be tested again in a higher number of patients, and additional parameters will be included in order to gain insights into the sperm physiological changes that underpin the improvement in semen quality
Status | Recruiting |
Enrollment | 100 |
Est. completion date | November 12, 2022 |
Est. primary completion date | November 12, 2022 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years to 45 Years |
Eligibility | Inclusion Criteria: - Age: 18 to 45 - Male patients with idiopathic infertility classified with asthenozoospermia, oligozoospermia or oligoasthenozoospermia after seminal assessment. - Not achieving pregnancy after at least one year of intercourse with the same partner without protective measures Exclusion Criteria: - Azoospermia (absence of spermatozoa) or severe oligozoospermia (< 5 million spermatozoa/ml of ejaculate) - Testicular torsion or prostatitis - Urinary retention and infections - Drug consumption - Hormone treatments - Recent surgical interventions - Diabetes - Kidney or liver disease - Leukocytosis - Antioxidant supplement consumption in the last 3 months - BMI >30 Kg/m2 - Endocrinopathies, hypo and hyperthyroidism - Chromosomal anomalies (XX, XYY, XXY) - Treatments with anticoagulants - Radiotherapy/Chemotherapy - Participation in another clinical study prior to inclusion in this study that could affect the objectives of the current study |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital Clinic | Barcelona | |
Spain | Hospital Clinic | Barcelona |
Lead Sponsor | Collaborator |
---|---|
Fitoplancton Marino, S.L. | Fertypharm, Fundacio Clinic Barcelona |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | MiOXSYS system as a diagnostic test of abnormal seminal parameters and DNA fragmentation | In addition to seminal parameters and DNA fragmentation, sORP will be also assessed using the MiOXSYS system. Then, potential correlations between these parameters will be analyzed to evaluate the usefulness of MiOXSYS as a cheap and fast prognostic test of male infertility | 90 days | |
Primary | Sperm motility | Sperm motility will be assessed according to the method described in the WHO laboratory manual for the examination and processing of human semen, 5th ed. Geneva: World Health Organization (2010) | 90 days | |
Primary | Sperm concentration | Sperm concentration will be determined according to the method described in the WHO laboratory manual for the examination and processing of human semen, 5th ed. Geneva: World Health Organization (2010) | 90 days | |
Primary | Sperm oxidative stress | Oxidative stress status will be evaluated by measuring: i) intracellular Reactive Oxygen Species (ROS; includes superoxide anion, hydroxyl radical, hydrogen peroxide), and ii) sperm DNA oxidation via quantification of 8-hydroxydeoxyguanosine (8-OHdG). Flow cytometry will be employed in both cases. | 90 days | |
Secondary | DNA integrity | DNA integrity/fragmentation will be evaluated using the COMET assay | 90 days | |
Secondary | Adverse effects | Any kind of adverse event attributable to TetraSOD® will be recorded during the duration of the trial | 90 days |
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