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NCT06263192 Clinical Trial

Pregnancy Prediction Using Anti-Müllerian Hormone in Intrauterine Insemination Cycles

Infertility, Female Clinical Trial

Official title:
Pregnancy Prediction in Non-sterile Patients After 4 Intrauterine Inseminations With Donor Using Anti-Müllerian Hormone

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06263192
Other study ID # AMH-IUI
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 1, 2020
Est. completion date May 1, 2023

Study information
Verified date February 2024
Source Clinica de la Mujer Medicina Reproductiva, Chile
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this study is to compare the cumulative pregnancy rates after 4 artificial inseminations with donor (IAD) in non-sterile women with plasma AMH levels > and < 1.1 ng/mL.

Recruitment information / eligibility
Status Completed
Enrollment 342
Est. completion date May 1, 2023
Est. primary completion date December 1, 2022
Accepts healthy volunteers
Gender Female
Age group 25 Years to 39 Years
Eligibility Inclusion Criteria: - IUI cycles with sperm donors either due to severe oligoasthenoteratozoospermia in the partner (defined as a motile sperm count (MSC) < 5 million in the ejaculate) or for social reasons, with up to 4 attempts accounted for. Exclusion Criteria: - BMI >30 - Infertility due to bilateral tubal factor - Endometriosis grade II-IV.

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Intrauterine insemination
Intrauterine insemination with sperm donors

Locations
Country Name City State
Spain Fertty International Barcelona

Sponsors (2)
Lead Sponsor Collaborator
Jose Antonio Moreno Universitat Autonoma de Barcelona

Country where clinical trial is conducted

Spain, 

Outcome
Type Measure Description Time frame Safety issue
Primary Cummulative pregnancy rate Pregnancy rate after 4 cycles of IUI 36 months
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