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Assessment of TetraSOD® Efficacy to Improve Semen Parameters in Men With Idiopathic Infertility

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04864314
Recruitment Status : Recruiting
First Posted : April 28, 2021
Last Update Posted : September 2, 2021
Sponsor:
Collaborators:
Fundacio Clinic Barcelona
Fertypharm
Information provided by (Responsible Party):
Fitoplancton Marino, S.L.

Brief Summary:
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

Condition or disease Intervention/treatment Phase
Infertility, Male Dietary Supplement: Marine microalgae Tetraselmis chuii with high Superoxide Dismutase (SOD) activity Dietary Supplement: Sham Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 100 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
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
Actual Study Start Date : May 12, 2021
Estimated Primary Completion Date : November 12, 2022
Estimated Study Completion Date : November 12, 2022


Arm Intervention/treatment
Placebo Comparator: Control group
Group supplemented with a daily dose of placebo
Dietary Supplement: Sham
Participants in the Control group will receive a daily dose of placebo in a capsule during 90 days. After treatment, the group will stop consumption of placebo and a wash-out period of three months will start

Experimental: Experimental group
Group supplemented with a daily dose of TetraSOD®
Dietary Supplement: Marine microalgae Tetraselmis chuii with high Superoxide Dismutase (SOD) activity
Participants in the Experimental group will receive a daily dose of 250 mg of TetraSOD® in a capsule during 90 days. After treatment, the group will stop consumption of TetraSOD® and a wash-out period of three months will start
Other Name: TetraSOD®




Primary Outcome Measures :
  1. Sperm motility [ Time Frame: 90 days ]
    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)

  2. Sperm concentration [ Time Frame: 90 days ]
    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)

  3. Sperm oxidative stress [ Time Frame: 90 days ]
    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.


Secondary Outcome Measures :
  1. DNA integrity [ Time Frame: 90 days ]
    DNA integrity/fragmentation will be evaluated using the COMET assay

  2. Adverse effects [ Time Frame: 90 days ]
    Any kind of adverse event attributable to TetraSOD® will be recorded during the duration of the trial


Other Outcome Measures:
  1. MiOXSYS system as a diagnostic test of abnormal seminal parameters and DNA fragmentation [ Time Frame: 90 days ]
    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



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Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   Male
Gender Based Eligibility:   Yes
Accepts Healthy Volunteers:   No
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04864314


Contacts
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Contact: Carlos Infante +34 956561079 carlos.infante@easyalgae.com
Contact: Carlos Unamunzaga +34 956561079 cue@easyalgae.com

Locations
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Spain
Hospital Clinic Not yet recruiting
Barcelona, Spain, 08036
Contact: Juan M Corral    +34 932275545    jmcorral@clinic.cat   
Contact: Meritxell Jodar    +34 932275510    mjodar@clinic.cat   
Sub-Investigator: Marta Guimerà         
Sub-Investigator: Juan M Mayorga-Torres         
Sub-Investigator: Antonio Alcaraz         
Sub-Investigator: Dolors Manau         
Sub-Investigator: Rafael Oliva         
Hospital Clinic Recruiting
Barcelona, Spain
Contact: Juan M Corral, Dr         
Sponsors and Collaborators
Fitoplancton Marino, S.L.
Fundacio Clinic Barcelona
Fertypharm
Investigators
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Principal Investigator: Juan M Corral, Doctor Hospital Clinic (Barcelona, Spain)
Principal Investigator: Meritxell Jodar, Doctor Hospital Clinic (Barcelona, Spain)
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Responsible Party: Fitoplancton Marino, S.L.
ClinicalTrials.gov Identifier: NCT04864314    
Other Study ID Numbers: 2020_TSOD_01
First Posted: April 28, 2021    Key Record Dates
Last Update Posted: September 2, 2021
Last Verified: August 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Fitoplancton Marino, S.L.:
TetraSOD®
Infertility
Additional relevant MeSH terms:
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Infertility
Infertility, Male
Superoxide Dismutase
Free Radical Scavengers
Antioxidants
Molecular Mechanisms of Pharmacological Action
Protective Agents
Physiological Effects of Drugs