G-IVF and Sperm Parameters

NCT ID: NCT05597631

Last Updated: 2023-08-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

118 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-10-31

Study Completion Date

2024-04-30

Brief Summary

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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.

Detailed Description

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Conditions

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Infertility, Male

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Control

Control

Group Type NO_INTERVENTION

No interventions assigned to this group

G-IVF PLUS

G-IVF PLUS

Group Type EXPERIMENTAL

G-IVF PLUS

Intervention Type DEVICE

Experimental

Interventions

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G-IVF PLUS

Experimental

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Patients producing a pre-clinical semen sample at the clinic

Exclusion Criteria

* Patients with known azoospermia
* Patients who have had a vasectomy
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Vitrolife

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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IASO Maternity and Gynecology Clinic

Marousi, , Greece

Site Status

Countries

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Greece

Central Contacts

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Susanna Apter, PhL

Role: CONTACT

+46701648828

Alexandra Spyrou

Role: CONTACT

+302106184030

Facility Contacts

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Alexandra Spyrou

Role: primary

+302106184030

Eftychia Sklavolia

Role: backup

Other Identifiers

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2022-GR-GIVFSP

Identifier Type: -

Identifier Source: org_study_id

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