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F-18 FES Imaging for Endometriosis
Phase 1 & 2
Waitlist Available
Led By Ann Packard, MD
Research Sponsored by Annie (Annie) T. Packard
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Premenopausal women (18-50) with endometriosis
Be between 18 and 65 years old
Must not have
Postmenopausal women
Unable to receive IV Gadolinium contrast for any reason (renal failure eGFR < 60, contrast allergy)
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
No Placebo-Only Group
Summary
This trial aims to improve the detection of endometriosis using a special imaging technique. This method uses a substance that lights up endometriosis tissue on scans, helping doctors diagnose the condition more accurately.
Who is the study for?
This trial is for premenopausal women aged 18-50 who have been diagnosed with endometriosis. It's not suitable for postmenopausal women, those too large to fit in a PET/MRI machine, anyone unable to undergo PET/MRI (due to metal implants or severe claustrophobia), those who can't receive IV Gadolinium contrast (due to kidney issues or allergies), or pregnant women.
What is being tested?
The study is testing the use of a special imaging technique called F-18 FES PET/MRI to see if it can better detect endometriosis in affected individuals compared to current methods.
What are the potential side effects?
Potential side effects may include reactions related to the IV Gadolinium contrast used during imaging, such as nausea, pain at injection site, and allergic reactions. The F-18 FES tracer itself may cause similar side effects but these are generally rare.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am a woman aged 18-50 with endometriosis.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am a woman who has gone through menopause.
Select...
I cannot have IV Gadolinium contrast due to kidney issues or an allergy.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Detection of Endometriosis
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: F-18 FES PET/MRIExperimental Treatment1 Intervention
16α-(18)F-fluoro-17β-estradiol (\[F-18\] FES)
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Endometriosis treatments often target hormonal pathways to reduce estrogen levels or block its effects, as estrogen promotes the growth of endometrial tissue. Common treatments include estrogen-progestin contraceptives, which suppress ovulation and reduce menstrual flow, and GnRH agonists/antagonists, which lower estrogen production by downregulating the pituitary gland.
Dienogest, a progestin, reduces endometrioma volume and pain by creating a hypoestrogenic environment. These treatments are crucial for managing symptoms and preventing disease progression.
The F-18 FES PET/MRI trial leverages the binding of a radiotracer to estrogen receptors, enhancing imaging of endometriotic lesions, which underscores the importance of understanding estrogen's role in endometriosis.
State of the art, new treatment strategies, and emerging drugs for non-hormonal treatment of endometriosis: a systematic review of randomized control trials.Pre and post operative medical therapy for endometriosis surgery.
State of the art, new treatment strategies, and emerging drugs for non-hormonal treatment of endometriosis: a systematic review of randomized control trials.Pre and post operative medical therapy for endometriosis surgery.
Find a Location
Who is running the clinical trial?
Annie (Annie) T. PackardLead Sponsor
Ann Packard, MDPrincipal InvestigatorMayo Clinic
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am a woman who has gone through menopause.I cannot have IV Gadolinium contrast due to kidney issues or an allergy.I am a woman aged 18-50 with endometriosis.
Research Study Groups:
This trial has the following groups:- Group 1: F-18 FES PET/MRI
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Endometriosis Patient Testimony for trial: Trial Name: NCT04347135 — Phase 1 & 2
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