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Artificial insemination with donor sperm: Intrauterine insemination or intracervical insemination? The AID study

Artificial insemination with donor sperm: Intrauterine insemination or intracervical insemination? The AID study - AID-study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON47048
Enrollment
396
Registered
2014-01-20
Start date
2014-06-03
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Artificial insemination donor sperm

Interventions

A maximum of six cycles IUI or ICI without the addition of ovarian stimulation in a time frame of 8 months.

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a subject must meet all the following criteria: Indications for AID o Couples with azoospermia o Couples with failed TESE procedure o Couples with a partner with a hereditary genetic defect o Lesbian couples o Single women - Regular cycle - Women with anovulation who become ovulatory after ovulation induction

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in tis study: - Double sided tubal pathology - women with a history of subfertility, other than male factor - Women younger than 18 or older than 43 years

Design outcomes

Primary

MeasureTime frame
The primary outcome is ongoing pregnancy leading to a live birth within a time horizon of eight months.

Secondary

MeasureTime frame
1. clinical pregnancy 2. miscarriage 3. multiple pregnancy 4. pregnancy complications (preterm birth, preeclampsia) 5. direct and indirect costs

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)