Ultrasound Guided Artificial Insemination - Full Text View

Ultrasound Guided Artificial Insemination (UGAI)

This study has been completed.

Sponsored by:	Hospital de Cruces
Information provided by:	Hospital de Cruces
ClinicalTrials.gov Identifier:	NCT00809952

Purpose

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

Condition	Intervention	Phase
Insemination	Procedure: recombinant FSH	Phase IV

MedlinePlus related topics: Ultrasound

Study Type:

Observational

Further study details as provided by Hospital de Cruces:

Groups/Cohorts	Assigned Interventions
Recombinat FSH	Procedure: recombinant FSH

Eligibility

Criteria

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:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00809952

Locations

Spain, Basque Country
Human Reproduction Unit
Cruces-Baracaldo, Basque Country, Spain, 48903

Sponsors and Collaborators

Hospital de Cruces

More Information

Study ID Numbers:	HUMREP-08-0656
Study First Received:	December 15, 2008
Last Updated:	December 15, 2008
ClinicalTrials.gov Identifier:	NCT00809952
Health Authority:	Spain: Ministry of Health

ClinicalTrials.gov processed this record on January 14, 2009