- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02990949
The Impact of the Timing of Trigger on IVF Success
October 12, 2022 updated by: Colorado Center for Reproductive Medicine
The Impact of the Timing of Trigger on IVF Success: Randomized Control Trial
The aim of this study is to examine the length of ovarian stimulation with the timing of trigger in an IVF cycle and its potential to impact patient outcomes.
Study Overview
Status
Terminated
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
29
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Colorado
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Lone Tree, Colorado, United States, 80124
- Colorado Center for Reproductive Medicine
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
26 years to 44 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Planning to move forward with an IVF cycle
- Have met the requirements of being a patient at CCRM Colorado
- AMA: 39-44 years old And/or
- DOR: AMH < 1 & FSH >10 (age independent)
Exclusion Criteria:
- Contraindication for pregnancy
- Have not fulfilled requirements for IVF cycle
- Single gene couple or chromosomal rearrangement
- Severe male factor or testicular surgical sperm removal (need sufficient sperm for ICSI)
- One ovary
- Uterine anomalies
- Stage III or IV endometriosis
- Explained recurrent miscarriage
- PCO or PCOS
- Using donor oocyte or gestational carrier
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control group
|
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Experimental: Testing group
Timing of trigger at end of ovarian stimulation in an IVF cycle: trigger when 2 follicles reach 18mm, OR 1 follicle reaches 18mm AND 1 follicle is between 16-18mm.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Euploid Embryos: the percentage of euploid embryos produced as analyzed by comprehensive chromosomal screening, of total embryos tested
Time Frame: 4 weeks after egg retrieval
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4 weeks after egg retrieval
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Egg maturation: the proportion of mature eggs of total number of eggs retrieved
Time Frame: 1 week after egg retrieval
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1 week after egg retrieval
|
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Live birth outcomes: the incidence of pregnancy resulting in live birth following embryo transfer of embryos produced by this IVF cycle
Time Frame: 9 months after frozen embryo transfer
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9 months after frozen embryo transfer
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Director: Mandy Katz-Jaffe, PhD, CCRM, FLC
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
November 1, 2016
Primary Completion (Actual)
May 9, 2022
Study Completion (Actual)
June 15, 2022
Study Registration Dates
First Submitted
December 6, 2016
First Submitted That Met QC Criteria
December 9, 2016
First Posted (Estimate)
December 13, 2016
Study Record Updates
Last Update Posted (Actual)
October 14, 2022
Last Update Submitted That Met QC Criteria
October 12, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20160397
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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