- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05842070
The Stanford Egg Freezing Study
The Stanford Egg Freezing Study: Investigating a Low-Cost, Low-Intensity Oocyte Cryopreservation Protocol
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The 2020-2025 strategic plan of ASRM lists equitable, affordable access to reproductive healthcare as a high-focus priority goal, with a pressing need to identify cost-effective treatments that patients shut out by finances can still afford. While there have been some efforts made to broaden access to infertility treatment with in-vitro fertilization (IVF), there are very limited efforts to do for patients desiring egg freezing as a strategy for deferred reproduction. The Stanford Egg Freezing Study is a novel clinical trial that will be assessing for non-inferiority of outcomes from a low-cost, low-intensity approach called the Cardinal Protocol, compared to the routinely used high-intensity clinic protocols. Participant enrollment will occur locally in the greater Bay Area from patients pursuing egg freezing for fertility preservation at Stanford's Fertility clinic.
To specifically review the Cardinal Protocol, this is a low-cost, low-intensity egg-freezing protocol designed to be cost-conscious and streamlined compared to all the other routine protocols used in clinic. This means medication doses are protocolized, decreasing the total number of injections and medications needed, bloodwork and ultrasounds are limited, prevention of premature ovulation is done using oral progestins, and trigger timing is standardized as opposed to timed by provider preference, resulting in a projected cost-savings of on average $5,800 ($3,700-$11,000). This protocol has been reviewed and approved by all 8 REI board-certified infertility specialists at Stanford who based on the literature and practice deem this a standard protocol that could be offered to patients interested in a lower-cost approach.
The investigators hypothesize that the Cardinal protocol compared to the other routinely used high-intensity clinic protocols, will offer non-inferior clinical outcomes for patients with respect to the number of eggs retrieved, improve overall patient satisfaction, and decrease out-of-pocket costs, as well as time required off work to complete the treatment.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
California
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Sunnyvale, California, United States, 94087
- Stanford Fertility and Reproductive Health Services
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Ovary-bearing individuals of reproductive age 18-40, interested in pursuing OC
- AMH > 0.3 ng/mL
- AMH < 7 ng/mL
Exclusion Criteria:
- AMH > 7 ng/mL or physician concern for risk of developing severe OHSS
- History of severe OHSS
- Severe diminished ovarian reserve (DOR) def. as AMH < 0.3 ng/mL or FSH > 15
- BMI > 45
- Any contraindications to ovarian stimulation or outpatient egg retrieval under anesthesia
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Low-Intensity Protocol
Participants choose the low-cost, low-intensity egg-freezing protocol
|
The low-intensity egg freezing protocol involves fewer ultrasounds, bloodwork and injections, contributing to a lower cost.
Otherwise, this protocol does not differ significantly from the other routine high-intensity clinic protocols.
Other Names:
|
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Active Comparator: High-intensity protocol
Participants choose a routine high-intensity egg-freezing protocol
|
The high-intensity egg freezing protocol is a routinely used clinic protocol where patients are coming for frequent ultrasounds and bloodwork, as well as more injections, contributing to a higher overall cost for egg-freezing.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oocyte yield per retrieval or egg freezing cycle
Time Frame: Identified within 24 hours of the oocyte retreival
|
Number of oocytes retrieved
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Identified within 24 hours of the oocyte retreival
|
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Mature oocytes cryopreserved per egg freezing cycle
Time Frame: Identified within 24-48 hours of the oocyte retreival
|
Number of mature oocytes cryopreserved
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Identified within 24-48 hours of the oocyte retreival
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Participant satisfaction with egg freezing experience and specific protocol (assessed using the Likert scale)
Time Frame: Identified on post-cycle survey completed 1-2 months following oocyte retrieval
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Assessment of satisfaction on scale of 1-5 towards egg freezing process and protocol
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Identified on post-cycle survey completed 1-2 months following oocyte retrieval
|
|
Out-of-pocket costs of the egg freezing cycle for the participant
Time Frame: Identified on post-cycle survey completed 1-2 months following oocyte retrieval and via the electronic medical record
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With or without insurance coverage for egg freezing, with an assessment of total costs or charges of the cycle, including medication costs
|
Identified on post-cycle survey completed 1-2 months following oocyte retrieval and via the electronic medical record
|
|
Time off-work needed to complete the egg freezing cycle
Time Frame: Identified on post-cycle survey completed 1-2 months following oocyte retrieval
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Not including the egg retrieval procedure day
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Identified on post-cycle survey completed 1-2 months following oocyte retrieval
|
|
Additional cost per additional oocytes retrieved
Time Frame: Identified from post-cycle survey completed 1-2 months following oocyte retrieval
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Cost-benefit analyses
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Identified from post-cycle survey completed 1-2 months following oocyte retrieval
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ruth Lathi, MD, Stanford University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69100
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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