Assisted Reproductive Techniques (ART) With Sperm Donation : an Inclusive

Status Recruiting

Clinical Trial Summary

This is a monocentric, retrospective, non-interventional study. The main objective is to describe the populations requesting assisted reproductive techniques (ART) with sperm donation ; and compare them between groups depending on their parental project.. The secondary objectives are to describe the center support process in the context of ART with sperm donation, to determine the initial/final orientation of support and the time to care The statistical analysis will be carried out to compare these parameters between groups depending on their parental project The study is taking place in the reproductive medicine department of the regional university hospital centre in Nancy.

Clinical Trial Description

Descriptive analysis of a new MAP population since the update of bioethics legislation in August 2021 This study is a descriptive analysis of the population requesting assisted reproductive techniques (ART) with sperm donation since update of bioethics legislation in August 2021 ; and compare them in groups depending on their parental project. The main objective is to describe the different populations requesting ART with sperm donation (number and evolution of requests, age, history, geographical origin, infertility delay, parenthood context). The secondary objectives are to describe the center support process in the context of ART with sperm donation, to determine the initial/final orientation of support and the time to care and compare them between groups depending on their parental project The statistical analysis will be carried out to compare these parameters between groups depending on their parental project This research contributes to our knowledge of patients with a parental project. It may lead to improve their medical care The study is monocentric, retrospective, non-interventional and does not involve human subjects. This research is based on existing data, extracted from patient files in the médifirst software. This is taking place in the reproductive medicine department of the regional university hospital centre in Nancy. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06163079
Study type	Observational
Source	Central Hospital, Nancy, France
Contact	Agopiantz Mikael, PhD
Phone	0033383344426
Email	mikael.agopiantz@gmail.com
Status	Recruiting
Phase
Start date	March 1, 2023
Completion date	April 2024

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Assisted Reproductive Techniques (ART) With Sperm Donation : an Inclusive Model of ART for All Women — PMAPT

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms