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Ultrasound Guided Artificial Insemination

NCT ID: NCT00809952

Last Updated: 2008-12-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Study Classification

OBSERVATIONAL

Brief Summary

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

Detailed Description

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Conditions

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Insemination

Study Groups

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Recombinat FSH

recombinant FSH

Intervention Type PROCEDURE

Interventions

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recombinant FSH

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hospital de Cruces

OTHER

Sponsor Role lead

Locations

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Human Reproduction Unit

Cruces-Baracaldo, Basque Country, Spain

Site Status

Countries

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Spain

References

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Ramon O, Matorras R, Corcostegui B, Meabe A, Burgos J, Exposito A, Crisol L. Ultrasound-guided artificial insemination: a randomized controlled trial. Hum Reprod. 2009 May;24(5):1080-4. doi: 10.1093/humrep/den498. Epub 2009 Feb 5.

Reference Type DERIVED
PMID: 19196748 (View on PubMed)

Other Identifiers

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HUMREP-08-0656

Identifier Type: -

Identifier Source: org_study_id