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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05597631
Other study ID # 2022-GR-GIVFSP
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date October 2023
Est. completion date April 2024

Study information

Verified date August 2023
Source Vitrolife
Contact Susanna Apter, PhL
Phone +46701648828
Email sapter@vitrolife.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate if adding a fixed volume of a physiological solution to a freshly produced sperm sample will affect sperm characteristics.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 118
Est. completion date April 2024
Est. primary completion date March 2024
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Patients producing a pre-clinical semen sample at the clinic Exclusion Criteria: - Patients with known azoospermia - Patients who have had a vasectomy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
G-IVF PLUS
Experimental

Locations

Country Name City State
Greece IASO Maternity and Gynecology Clinic Maroussi

Sponsors (1)

Lead Sponsor Collaborator
Vitrolife

Country where clinical trial is conducted

Greece, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of progressive motile sperm (%) Proportion of progressive motile sperm after sample preparation 10 minutes of assessment will be used to count the motile sperm for each sample.
Secondary Sperm yield (%) Percentage of total number of motile sperm after sperm preperation 10 minutes used to assess motilty (as for primary outcome)
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