The Aim of This Study is to Determine the Incidence of Alterations in Fluorescent In Situ Hybridisation (FISH) of Spermatozoa and to Evaluate the Efficacy of the Use of Annexin Columns (MACS®) in Patients With Altered FISH Undergoing In Vitro Fertilisation Techniques

Not Applicable

Completed

• Conditions: Infertility, Male
• Interventions: Device: Magnetic Activated Cell Sorting

• Registration Number: NCT06524102
• Lead Sponsor: Instituto de Investigación Sanitaria y Biomédica de Alicante

Brief Summary

250 petitions for FISH of spermatozoa were requested, determining the total and particular incidence in each of the indications collected. The effect of annexin columns was evaluated in 10 couples with altered FISH. In each of the couples, oocytes were pseudo-randomised to the control group and MACS®. All couples received experimental treatment. Mixed logistic regression model were adjusted to evaluate the effect of MACS® on the response variables studied.

Detailed Description

Prospective pseudo-randomised study carried out in the reproduction unit of the Hospital General Universitario Dr. Balmis in Alicante. The study was divided into two phases, with both being conducted in parallel. The research was approved by the Ethics Committee for Research on Medicines (CEIm) of the Alicante Department of Health. The treatment and use of the clinical data required for this study complied with current legislation, preserving the anonymity of the patients.

Phase I. A total of 250 sperm FISH tests were requested for different indications in men aged 18-55 years with normal karyotype. Of the total number of tests requested, 16 could not be performed due to low sperm count. Finally, 234 samples were analysed, of which 20 had altered sperm FISH.

Phase II. From the previous phase, not all patients with an altered FISH test were included in the second phase of the study, some of them were lost for different reasons (n=10). A total of 10 couples with no previous children in common, negative serology and normal karyotype were included. Females were aged less than 40 years and males less than 50 years at the time of treatment.

The semen sample of each couple was capacitated by density gradient centrifugation (DGC) and swim up, forming the control group. An aliquot was taken that was destined to pass through the annexin columns (MACS® ART, Miltenyl Biotic GmbH, Germany) constituting the study group. The oocytes obtained in each of the couples were pseudo-randomized and inseminated by ICSI with sperm from the study group and the control group. All couples benefited from the experimental treatment since they had the opportunity to inseminate their oocytes with sperm from both groups, thus excluding treatment bias or asymmetry.

To evaluate the efficacy of MACS® on laboratory outcome, fertilization rates, abnormal fertilization, biopsiable embryos and euploid embryos were compared between the study and control group.

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2018-01-01
• Primary Completion: 2022-03-31
• Study Completion: 2022-03-31
• Status Verified: 2024-07
• Study First Submitted: 2024-07-21
• Study First Submitted QC: 2024-07-25
• Last Update Submitted: 2024-07-25
• Study First Posted: 2024-07-29
• Last Update Posted: 2024-07-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Women between 18 and 40 years of age. Men between 18 and 55 years of age.
• Couples without any common, previous and healthy children.
• Couples with indication of IVF-ICSI cycle with Preimplantation Genetic Test for Aneuploidy (PGT-A).
• Men with altered sperm FISH results.

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Exclusion Criteria

• Prior voluntary sterilization.
• Existence of documented medical contraindication for infertility treatment.
• Existence of documented medical contraindication to pregnancy.
• Existence of a documented medical situation that seriously interferes with the development of the offspring.
• Impossibility to comply with the treatment for health-related reasons or other family or social environment-related reasons.
• Existence of a documented situation referring to any other circumstance that may seriously interfere with the development of the offspring submitted for consideration to a health care ethics committee or similar body.
• One or both partners with positive serology for HIV, HBV and VDRL.
• One or both partners with partner with altered karyotype.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
MACS	Magnetic Activated Cell Sorting	Oocytes corresponding to this group were inseminated by spermatozoa selected after the use of MACS.

Primary Outcome Measures

Name	Time	Method
Euploid embryo rate	This variable was taken 2 days after obtaining the genetic result of the embryo biopsy.	Embryos without chromosomal alterations in relation to the total number of those that were informative.

Secondary Outcome Measures

Name	Time	Method
Fertilization rate	This variable was taken 17-20 hours after oocyte insemination.	Number of correctly fertilized zygotes among the total number of mature oocytes inseminated
Biopsiable embryo rate	This variable was taken on the 3rd day of embryonic development, at the time of the embryo biopsy. .	Number of biopsied embryos versus the total number of correctly fertilized zygotes

Trial Locations

Locations (1)

ISABIAL; 🇪🇸 Alicante, Spain