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Ultrasound Guided Artificial Insemination

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00809952
Acronym
UGAI
Enrollment
Unknown
Registered
2008-12-17
Start date
Unknown
Completion date
Unknown
Last updated
2008-12-17

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

Conditions

Insemination

Brief summary

The purpose of this study is to ascertain whether using ultrasound guidance during intrauterine insemination (IUI) could increase pregnancy rates.

Interventions

Sponsors

Hospital de Cruces
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* The woman's inclusion criteria in our IUI program were at least one patent tube, normal cavity, basal FSH \< 10 mU/mL and age under 40 years. * IUI with husband's sperm (IUI-H) was indicated when, after sperm preparation, at least 5 million motile spermatozoa were recovered; this was performed in 58 cases (79.45%). * In the remaining 15 cases (20.55%), IUI was performed with donor sperm (IUI-D) either because of azoospermia (n=6) failure to recover spermatozoa during testicular biopsy (n=5) or in women without a male partner (n=4).

Exclusion criteria

* Previous infertility treatments had been carried out.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026