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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03132818
Other study ID # RNI2016-25 Dr Scheffler
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date July 20, 2017
Est. completion date February 20, 2019

Study information

Verified date July 2020
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Sexual disorders associated with medical aid for procreation have already been demonstrated in several studies. However, few of them are interested in the problem of patients in charge of donating gametes, and if studied, it is often restricted to donating sperm to a small number of patients. For this reason, it would be interesting to study the impact of the intake and in charge and the treatments of the Medical Aid to the Procreation on this population of patients (including the patients treated in donation of sperm but also Those supported in oocyte donation)


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 20, 2019
Est. primary completion date February 20, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Couple, male and female, meeting the legal criteria for access to medically assisted procreation: a couple, a woman under the age of 43, who can testify to a life together. Then breakdown into 3 inclusion groups:

- Group 1: Patients undergoing AMP with oocyte donation

- Group 2: couples supported in AMP with sperm donation

- Group 3: torque supported in intra torque AMP.

Exclusion Criteria:

- Patients who do not meet the legal criteria for access to the MPA.

- Patients in charge of Medical Assistance for Procreation "Viral Risk"

- Patients undergoing medical aid for procreation for pre-existing sexual dysfunction.

- Patients awaiting embryo reception.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
To evaluate the prevalence of sexual disorders in patients receiving AMP
To evaluate the prevalence of sexual disorders in patients receiving AMP

Locations

Country Name City State
France CHU Amiens Picardie Amiens Picardie

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Analysis of anonymous sexual well-being questionnaires: one reserved for men, another reserved for women Analysis of anonymous sexual well-being questionnaires: one reserved for men, another reserved for women 1 year
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