Ultrasound Guided Artificial Insemination

Insemination Clinical Trial

— UGAI  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00809952
• Other study ID #: HUMREP-08-0656
• Status: Completed
• Phase: Phase 4
• First received: December 15, 2008
• Last updated: December 15, 2008

Study information

• Verified date: December 2008
• Source: Hospital de Cruces
• Contact: n/a
• Is FDA regulated: No
• Health authority: Spain: Ministry of Health
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years to 40 Years

Eligibility

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.

Study Design

N/A

Related Conditions & MeSH terms

• Insemination

Intervention

Procedure:
• recombinant FSH

Locations

Country	Name	City	State
Spain	Human Reproduction Unit	Cruces-Baracaldo	Basque Country

Sponsors (1)

Lead Sponsor	Collaborator
Hospital de Cruces

Country where clinical trial is conducted

Spain,