Chicago, ILNCT07286188Now EnrollingIRB Ready

Fibroids, Uterine Clinical Trial in Chicago, IL

Access cutting-edge fibroids, uterine treatment through this clinical trial at a research site in Chicago. Study-provided care at no cost to qualified participants.

Sponsored by Northwestern University

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Expert Care in Chicago

Access fibroids, uterine specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related fibroids, uterine treatment provided free

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Check if you qualify for this fibroids, uterine clinical trial in Chicago, IL

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Why Participate?

  • No-Cost Study Care

  • Local to Chicago

    Convenient for IL residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Chicago site if eligible
  4. 4Begin participation

About This Fibroids, Uterine Study in Chicago

The goal of this double blinded randomized control trial is to evaluate the impact of misoprostol on fluid deficit during hysteroscopic myomectomies. The main questions it aims to answer are: Is there is difference in fluid deficit in patients who receive misoprostol vs placebo pre operatively for hysteroscopic myomectomies? Participants will be randomized to received 800 mcg of either rectal misoprostol prior to their hysteroscopic myomectomy or 4 tablets of placebo (ZEEBO) prior to their hysteroscopic myomectomy.

Sponsor: Northwestern University

Who Can Participate

Inclusion Criteria

Patients presenting for hysteroscopic myomectomy for uterine fibroids on pelvic imaging (pelvic ultrasound or MRI) within in last 12 months
Age ≥ 18 years and ≤ 50 years.
Fibroids between 1-3cm in size
Myomectomy using myosure or resectoscope devices
Willing to have rectal misoprostol or placebo at time of procedure
Ability to understand and the willingness to sign a written informed consent.
Admissible medical/surgical history.
Can be previously treated with Depo-Lupron, Depo-Provera, or Oral Contraceptive pills
Can have had prior Cesarean delivery

Exclusion Criteria

Pregnancy. All patients will be required to have a negative urine pregnancy test prior to surgery.
Post-menopausal women.
Patients with a history of gynecologic malignancy.
History of allergic reactions attributed to compounds of similar chemical or biologic composition to misoprostol.
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Known active inflammatory bowel disease involving the rectum or other significant anorectal conditions that may interfere with safe rectal administration of study medication.

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 Chicago?

Yes, this clinical trial (NCT07286188) has an active research site in Chicago, IL 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.

Fibroids, Uterine Treatment Options in Chicago, IL

If you're searching for fibroids, uterine treatment options in Chicago, IL, this clinical trial (NCT07286188) 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 Chicago research site is actively enrolling participants for this clinical trial. You'll receive care from experienced fibroids, uterine 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 fibroids, uterine clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Chicago, IL