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Diagnostic Test

AdhesioRT for Infertility (AdhesioRT Trial)

N/A
Waitlist Available
Led By Isaac-Jacques Kadoch, MD
Research Sponsored by Clinique Ovo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Women between the ages of 18 to 40 inclusive at the time of oocyte retrieval
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days after embryo transfer
Awards & highlights

AdhesioRT Trial Summary

This trial is testing a new way to help an embryo implant in the uterus, which may help improve the success rate of pregnancy for people undergoing assisted reproductive techniques.

Who is the study for?
This trial is for women aged 18-40 who are undergoing fertility treatments and have at least two high-quality frozen embryos ready for transfer. They must not be preserving fertility for future use, have severe endometriosis or uterine abnormalities, nor test positive for HIV, Hepatitis B (unless from vaccination), or Hepatitis C.Check my eligibility
What is being tested?
The study tests AdhesioRT to personalize the window of implantation during a single frozen embryo transfer in an attempt to improve pregnancy establishment rates by enhancing uterine receptivity.See study design
What are the potential side effects?
Potential side effects are not explicitly listed but may include typical risks associated with embryo transfers such as infection, bleeding, or complications related to hormonal treatments used in the process.

AdhesioRT Trial Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I am a woman aged 18 to 40.

AdhesioRT Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 days after embryo transfer
This trial's timeline: 3 weeks for screening, Varies for treatment, and 14 days after embryo transfer for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Determination of appropriate window of implantation
Secondary outcome measures
Rate of clinical pregnancy

AdhesioRT Trial Design

2Treatment groups
Active Control
Group I: Study Group - AdhesioRTActive Control1 Intervention
Prior to frozen embryo transfer, participants will proceed with the AdhesioRT test. Participants randomized in the study group will proceed with frozen embryo transfer cycle according window of implantation determined by AdhesioRT.
Group II: Control Group - Standard of CareActive Control1 Intervention
Prior to frozen embryo transfer, participants will proceed with the AdhesioRT test. Participants randomized in the control group will proceed with the first frozen embryo transfer cycle as per standard of care. In the event of unsuccessful implantation (negative serum pregnancy test), participants will proceed with subsequent frozen embryo transfer cycle according to window of implantation determined by AdhesioRT.

Find a Location

Who is running the clinical trial?

Ferring PharmaceuticalsIndustry Sponsor
314 Previous Clinical Trials
440,765 Total Patients Enrolled
60 Trials studying Infertility
32,202 Patients Enrolled for Infertility
Clinique OvoLead Sponsor
31 Previous Clinical Trials
41,387 Total Patients Enrolled
19 Trials studying Infertility
8,207 Patients Enrolled for Infertility
Isaac-Jacques Kadoch, MDPrincipal InvestigatorClinique Ovo
1 Previous Clinical Trials
800 Total Patients Enrolled

Media Library

AdhesioRT (Diagnostic Test) Clinical Trial Eligibility Overview. Trial Name: NCT04840121 — N/A
Infertility Research Study Groups: Study Group - AdhesioRT, Control Group - Standard of Care
Infertility Clinical Trial 2023: AdhesioRT Highlights & Side Effects. Trial Name: NCT04840121 — N/A
AdhesioRT (Diagnostic Test) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04840121 — N/A
~29 spots leftby May 2025
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