- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06128395
ASA 81 mg vs 162 mg During Frozen Embryo Transfer (FET)
December 3, 2025 updated by: Clinique Ovo
Retrospective Study to Assess if Aspirin 162 mg is Better Than 81 mg for Embryo Transfer Outcomes
The use of low dose aspirin is recommended for high risk patients to reduce the risk of pre-eclampsia, placental abruption and antepartum hemorrhage.
Recent studies have shown that in a specific population, the use of low dose aspirin might reduce the risk of preterm birth in pregnant women with singleton pregnancy.
In June 2022, clinique ovo started implementing the use of Aspirin 162 mg instead of 81 mg in the frozen embryo transfer cycles based on recent study outcomes.
The use of Aspirin 162 mg might have additional benefits on the embryo transfer outcomes by decreasing the miscarriage.
Moreover this can be continued until late in pregnancy without adverse effects.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
1207
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
-
-
Quebec
-
Montreal, Quebec, Canada, H4P 2S4
- Clinique ovo
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
FET Data spreadsheet from January 2022 to December 2022
Description
Inclusion Criteria:
- Women taking aspirin 81 mg or 162 mg prior to an autologous embryo transfer
- Age < 40 years old
- Embryo transfer cycle done at clinique ovo
Exclusion Criteria:
- Egg or embryo recipient
- History of recurrent miscarriages, defined as ≥ 3 consecutive losses
- Patients that needed Viagra, PRP or other modalities to improve their endometrial thickness
- Uterine factor infertility
- Abnormal hormonal profiles
- Stimulated embryo transfer cycles
- History of recurrent implantation failure defined as failed ≥ 2 euploid embryos transfer or ≥ 3 blastocysts
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Aspirin 81 mg for Frozen Embryo Transfer (FET)
Subjects were prescribed Aspirin 81 mg to be started on the third day of their menstrual cycle in preparation for their FET.
|
A frozen embryo transfer involves thawing a fertilized embryo and transferring it in the uterus in order to obtain a pregnancy
|
|
Aspirin 162 mg for Frozen Embryo Transfer (FET)
Subjects were prescribed Aspirin 162 mg to be started on the third day of their menstrual cycle in preparation for their FET
|
A frozen embryo transfer involves thawing a fertilized embryo and transferring it in the uterus in order to obtain a pregnancy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Compare clinical pregnancy rate between patients prescribed Aspirin 81 mg vs Aspirin 162 mg
Time Frame: Time Frame: 6 to 8 weeks after Frozen Embryo Transfer
|
clinical pregnancy is the presence of fetal heartbeat at the viability ultrasound
|
Time Frame: 6 to 8 weeks after Frozen Embryo Transfer
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Wael Jamal, MD, Clinique ovo
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, 2023
Primary Completion (Actual)
August 30, 2024
Study Completion (Actual)
September 18, 2024
Study Registration Dates
First Submitted
November 7, 2023
First Submitted That Met QC Criteria
November 7, 2023
First Posted (Actual)
November 13, 2023
Study Record Updates
Last Update Posted (Estimated)
December 9, 2025
Last Update Submitted That Met QC Criteria
December 3, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 3384
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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