search
Back to results

Power Prenatal Supplements for Sperm Quality

Primary Purpose

Spermatogenesis and Semen Disorders, Infertility, Male

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Power Prenatal for Sperm
Sponsored by
The Bird and Be Co Inc
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spermatogenesis and Semen Disorders

Eligibility Criteria

18 Years - 45 Years (Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Male
  • Age 18-45 years old
  • Experiencing infertility
  • A recent semen analysis confirming low count, motility or morphology (at least 1 of 3) - within last 3 months

    1. Low concentration: < 15 Million / mL
    2. Low Motility: Progessive Motility < 30%
    3. Morphology: Strict criteria: Normal forms < 4% Reference: WHO 2020 6th edition: https://www.who.int/publications/i/item/9789240030787

Exclusion Criteria:

  • No diagnosed varicocele
  • Younger than 18 years old
  • Older than 45 years old
  • Currently taking any form of antioxidant supplements(in last 3 months) besides a general multivitamin

Sites / Locations

  • Reproductive Care CentreRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Power Prenatal for Sperm

Arm Description

This is a single arm study. Participants will take supplements for 3 months. The supplements is Power Prenatal for Sperm (active ingredients - https://birdandbe.com/the-power-prenatal-for-sperm)

Outcomes

Primary Outcome Measures

Sperm Progressive Motility (Semen Analysis); as percentage (%)
Semen analysis

Secondary Outcome Measures

Sperm Concentration (Semen Analysis); as millions / mL
Semen analysis
Sperm Morphology (Semen Analysis); as percentage (%)
Semen Analysis

Full Information

First Posted
June 5, 2022
Last Updated
August 20, 2023
Sponsor
The Bird and Be Co Inc
search

1. Study Identification

Unique Protocol Identification Number
NCT05410782
Brief Title
Power Prenatal Supplements for Sperm Quality
Official Title
A Three Month Course of Power Prenatal Supplements to Improve Sperm Quality in Male-factor Infertility Patients
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 1, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Bird and Be Co Inc

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
Male factor infertility is a leading cause of primary and secondary infertility. Poor sperm quality is defined as having an abnormal semen analysis [WHO 2020 - https://www.who.int/publications/i/item/9789240030787]. The effects of supplements (vitamins, minerals, and anti-oxidants) on improving sperm quality are still debated (https://pubmed.ncbi.nlm.nih.gov/30462179). Taking additional supplements to improve sperm quality represent a modifiable risk-factor that would be an easy intervention for patients struggling with male factor infertility. The life cycle of sperm production is estimated at 3 months, so any intervention would require a 3 month course to see its full effect. The investigators hypothesize that a 90 day course of the "Power Prenatal for Sperm", a male fertility supplement by Bird&Be (https://birdandbe.com/the-power-prenatal-for-sperm) will improve sperm quality based on semen analysis results prior to, and after taking the supplements.
Detailed Description
Male patients presenting to Conceive Health (https://conceivehealth.com/) or Reproductive Care Centre for infertility care will be potential candidates for this study. Male patients that have had a recent abnormal semen analysis conforming at least 1 of 3 parameters (low concentration: < 15 Million / mL; low progressive motility < 30%, and low morphology with strict criteria < 4%) will be eligible to participate. Patients will be approached by a study coordinator to participate in the study. The study coordinator will ensure all inclusion and exclusion criteria is met, consents forms are signed, and a 90 day course of the "Power Prenatal for Sperm" is dispensed Study participants will be instructed to repeat a semen analysis (at the same lab) after their 90 day course of the "Power Prenatal for Sperm". The differences between the semen analysis parameters will be compared The primary outcome was chosen as processive motility, as this parameter is mostly likely to be positively impacted by the Power Prenatal for Sperm. An abnormal progressive motility is defined as <5th percentile (32%) of the semen analysis of the fertile male population. The standard deviation for this population is 13.5%. The estimated effect size is 37.5%, from 32% to 44%, an increase of 12%. The alpha (type 1 error) significant level was set at 5% and the power level was set at 80%. The required sample size was 40 patients. Given that this study requires a 3 month intervention prior to a follow up semen analysis for comparison, the investigators estimated a 20% drop-out rate, so the total requirement was set at 50 patients. Table A1.2 (https://www.who.int/docs/default-source/reproductive-health/srhr-documents/infertility/examination-and-processing-of-human-semen-5ed-eng.pdf) Statistical analyses will be performed using standard expected methods. All data will be presented as mean ± Standard Deviation (SD). Statistical significance between semen analysis data will be determined by using the Shapiro-Wilk test of normality for predictions and paired samples t-test.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spermatogenesis and Semen Disorders, Infertility, Male

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients with male factor infertility, who have a document abnormal semen analysis (at least 1 of 3 abnormal parameters - concentration, progressive motility or morphology) will be recruited to take a 3 month course of supplements (Power Prenatal for Sperm), and a repeat semen analysis will be performed after the intervention to compare results
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Power Prenatal for Sperm
Arm Type
Experimental
Arm Description
This is a single arm study. Participants will take supplements for 3 months. The supplements is Power Prenatal for Sperm (active ingredients - https://birdandbe.com/the-power-prenatal-for-sperm)
Intervention Type
Dietary Supplement
Intervention Name(s)
Power Prenatal for Sperm
Other Intervention Name(s)
Prenatal Vitamins
Intervention Description
A prenatal vitamin complex that includes numerous ingredients aim at improving sperm quality (ingredients: https://birdandbe.com/the-power-prenatal-for-sperm)
Primary Outcome Measure Information:
Title
Sperm Progressive Motility (Semen Analysis); as percentage (%)
Description
Semen analysis
Time Frame
A repeat semen analysis will be performed 3 months after Power Prenatal for Sperm intervention
Secondary Outcome Measure Information:
Title
Sperm Concentration (Semen Analysis); as millions / mL
Description
Semen analysis
Time Frame
A repeat semen analysis will be performed 3 months after Power Prenatal for Sperm intervention
Title
Sperm Morphology (Semen Analysis); as percentage (%)
Description
Semen Analysis
Time Frame
A repeat semen analysis will be performed 3 months after Power Prenatal for Sperm intervention

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Male Age 18-45 years old Experiencing infertility A recent semen analysis confirming low count, motility or morphology (at least 1 of 3) - within last 3 months Low concentration: < 15 Million / mL Low Motility: Progessive Motility < 30% Morphology: Strict criteria: Normal forms < 4% Reference: WHO 2020 6th edition: https://www.who.int/publications/i/item/9789240030787 Exclusion Criteria: No diagnosed varicocele Younger than 18 years old Older than 45 years old Currently taking any form of antioxidant supplements(in last 3 months) besides a general multivitamin
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dan Nayot, Bsc, MSc, MD
Phone
4166163334
Email
dan@birdandbe.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dan Nayot, BSc, MSc, MD
Organizational Affiliation
The Bird and Be Co
Official's Role
Principal Investigator
Facility Information:
Facility Name
Reproductive Care Centre
City
Mississauga
State/Province
Ontario
ZIP/Postal Code
L5N 5S3
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dan Nayot, BSc, MSc, MD
Phone
905-816-9822
Ext
2403
Email
dnayot@rccfertility.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Power Prenatal Supplements for Sperm Quality

We'll reach out to this number within 24 hrs