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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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24 August 2015 |
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Main ID: |
NCT02526472 |
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Date of registration:
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13/08/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Transabdominal US-guided (UGET) vs. Modified Transvaginal US-guided (mTVET) Embryo Transfer in Human IVF
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Scientific title:
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A Large Prospective Randomized Trial Comparing Trans-abdominal Ultrasound-guided Embryo Transfer (UGET) With a Novel, Modified Trans-vaginal Ultrasound-guided Embryo Transfer Technique (mTVET) Based on Previous Uterine Length Measurement |
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Date of first enrolment:
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January 2012 |
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Target sample size:
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1648 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02526472 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Italy
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Contacts
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Name:
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Alberto Revelli, Prof. |
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Address:
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Telephone:
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Email:
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Affiliation:
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Dept. Surgical Sciences, Sant'Anna Hospital, University of Torino, Italy |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- patients undergoing autologous IVF
- ending IVF cycle with the transfer of fresh embryos
- treated at the investigators'r IVF Unit between Jan 2012 to Dec 2014
Exclusion Criteria:
- patients undergoing donor IVF
- ending IVF cycle without embryo transfer
- transferring frozen-thawed embryos
- treated elsewhere
Age minimum:
18 Years
Age maximum:
43 Years
Gender:
Female
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Health Condition(s) or Problem(s) studied
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Infertility
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Intervention(s)
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Procedure: ET under transabdominal US guidance (UGET)
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Procedure: ET after transvaginal US uterine measurement (mTVET)
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Primary Outcome(s)
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clinical pregnancy rate per embryo transfer (CPR/ET)
[Time Frame: 3 years]
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implantation rate
[Time Frame: 3 weeks (until the pregnancy test is performed)]
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Secondary Outcome(s)
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proportion of patients feeling moderate-to-severe discomfort during ET
[Time Frame: 3 years]
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Secondary ID(s)
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FDR-2-2015
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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