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G-IVF and Sperm Parameters

V

Vitrolife

Status

Not yet enrolling

Conditions

Infertility, Male

Treatments

Device: G-IVF PLUS

Study type

Interventional

Funder types

Industry

Identifiers

NCT05597631
2022-GR-GIVFSP

Details and patient eligibility

About

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.

Enrollment

118 estimated patients

Sex

Male

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Patients with known azoospermia
  • Patients who have had a vasectomy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

118 participants in 2 patient groups

Control
No Intervention group
Description:
Control
G-IVF PLUS
Experimental group
Description:
G-IVF PLUS
Treatment:
Device: G-IVF PLUS

Trial contacts and locations

1

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Central trial contact

Alexandra Spyrou; Susanna Apter, PhL

Data sourced from clinicaltrials.gov

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