Is NCT05058872 recruiting in Aurora, CO?

Yes, NCT05058872 is currently recruiting participants at its Aurora, CO location. This oral hormonal contraceptive use clinical trial is actively enrolling qualified participants.

How do I join the oral hormonal contraceptive use clinical trial in Aurora?

To join this clinical trial in Aurora, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Aurora clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

Oral Hormonal Contraceptive Use Clinical Trial in Aurora, CO

About This Oral Hormonal Contraceptive Use Study in Aurora

Purpose of this study: The purpose of this study is to learn more about how hormonal oral contraceptives affect brain processes and emotional wellbeing. Procedures: If participants agree to participate, the following will happen: 1. Eligibility visit (remote screening session) 2. If participants are eligible to participate in the study, they will be placed in one of two groups. If they are in the first group, they will be asked to take an oral contraception pill ("study drug") every day for 21 days. If they are in the second, they will take a placebo every day for 21 days. A placebo is a pill that looks like medicine but is not real and will have no medical effect on participants. Participants will not get to choose which group they are in, nor will they be told which group they are in. 3. During the three-week period in which participants will take either the study drug or placebo, they will be asked to complete daily check-in surveys on their computer or mobile device. 4. Participants will be asked to attend two additional visits over the course of about three weeks. At these visits, participants will be asked to undergo a urine drug screen, a blood draw, and a magnetic resonance imaging (MRI). They will also be asked to complete behavioral questionnaires.

Sponsor: University of Colorado, Denver

Who Can Participate

Inclusion Criteria

Aged 18 and older;

Right-handed;

Assigned female at birth;

Regular 21-35 day menstrual cycles for the past 6 months per self-report;

In generally good health per self-report. Those with a chronic medical condition may participate at the discretion of the principal investigator if the condition is stable;

Willingness to abstain from intercourse or use a non-hormonal back-up method of contraception (e.g., condoms) during the entire course of the study;

Negative urine drug screen, excepting marijuana or benzodiazepine that is being prescribed by a physician as a sleep aid, assessed at the baseline visit;

Ability to abstain from caffeine and/or cannabis for 2 hours prior to functional Magnetic Resonance Imaging (fMRI) scan visits;

Access to a reliable internet connection or cell phone data to complete daily questionnaires;

For those wishing to complete study screening session remotely: access to a reliable internet connection, computer to complete electronic consent and a private space to complete the session.

Exclusion Criteria

Presence or history of severe or unstable physical, neurological (per health history interview) or psychiatric disorders (assessed by Miniature International Neuropsychiatric Interview (MINI) but per Diagnostic and Statistical Manual of Mental Disorders - fifth edition (DSM-V) criteria, and the discretion of the principal investigator);

Lifetime history of psychotic disorders;

History of substance use disorder that has not been in remission (as defined by a substance free period of at least one year). However, individuals with mild disorders, disorders solely limited to cannabis, and/or those who have achieved close to one year of remission may be eligible at the discretion of the PI;

Presence or history of any category 3 or 4 conditions or medications per the CDC's (Centers for Disease Control and Prevention) Medical Eligibility Criteria for Contraceptive Use pertaining to combined hormonal contraceptive methods as per self-report and reviewed by the principal investigator;

Irregular menstrual periods per self-report;

Any current tobacco smoking (former smokers are eligible so long as their quit date was greater than one year ago);

Any personal or family history of a venous thromboembolism;

Known diagnosis of hypertensive disorder;

Any current or past history of malignancy;

Migraines with aura;

Systolic blood pressure greater than or equal to 140 or diastolic pressure greater than or equal to 90 taken at baseline visit;

Currently nursing an infant;

Known chromosomal or hormonal disorder affecting sex steroids;

Use of hormonal contraceptives currently or in the past 3 months, or use of medications that directly affect sex hormones (i.e. gonadotropin releasing hormone agonists, selective estrogen receptor modifiers);

Current pregnancy or pregnancy/delivery in the past six months;

Intention to become pregnant during study participation;

Current use of psychotropic medication;

Claustrophobia;

Metal in body unsafe for magnetic resonance imaging;

Weight over 300 pounds;

Conditions that would make magnetic resonance imaging unsafe for participants (i.e. aneurysm clip, cardiac pacemaker, etc.).

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Aurora?

Yes, this clinical trial (NCT05058872) has an active research site in Aurora, CO that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Oral Hormonal Contraceptive Use Treatment Options in Aurora, CO

If you're searching for oral hormonal contraceptive use treatment options in Aurora, CO, this clinical trial (NCT05058872) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Aurora research site is actively enrolling participants for this clinical trial. You'll receive care from experienced oral hormonal contraceptive use specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all oral hormonal contraceptive use clinical trials near you to find additional studies recruiting in your area.

Oral Hormonal Contraceptive Use Clinical Trial in Aurora, CO

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