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OpenTrials
Completed

NCT Number: NCT00809952

Ultrasound Guided Artificial Insemination

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

Completed

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Key information

Conditions

Insemination

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Human Reproduction Unit

Cruces-Baracaldo, Basque Country, 48903, Spain

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

recombinant FSH

Procedure

Sponsors and collaborators

Lead sponsor

Hospital de Cruces

Other

Registry information

Acronym: UGAI

Important dates

First posted
Dec 17, 2008
Registry last updated
Dec 17, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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