Ultrasound Guided Artificial Insemination (UGAI)
This study has been completed.
Sponsor:
Hospital de Cruces
Information provided by:
Hospital de Cruces
ClinicalTrials.gov Identifier:
NCT00809952
First received: December 15, 2008
Last updated: NA
Last verified: December 2008
History: No changes posted
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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 4 |
| Study Type: | Observational |
Further study details as provided by Hospital de Cruces:
Eligibility| Ages Eligible for Study: | 18 Years to 40 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
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:
- Previous infertility treatments had been carried out.
Contacts and Locations More Information
No publications provided by Hospital de Cruces
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| ClinicalTrials.gov Identifier: | NCT00809952 History of Changes |
| Other Study ID Numbers: | HUMREP-08-0656 |
| Study First Received: | December 15, 2008 |
| Last Updated: | December 15, 2008 |
| Health Authority: | Spain: Ministry of Health |
ClinicalTrials.gov processed this record on May 23, 2013