Providence, RINCT06969326Now EnrollingIRB Ready

Postoperative Bleeding Clinical Trial in Providence, RI

Access cutting-edge postoperative bleeding treatment through this clinical trial at a research site in Providence. Study-provided care at no cost to qualified participants.

Sponsored by Women and Infants Hospital of Rhode Island

Quick Self-Assessment

See if you qualify for this Providence location

Preparing your pre-screening questions…

Expert Care in Providence

Access postoperative bleeding specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related postoperative bleeding treatment provided free

Apply for This Providence Location

Check if you qualify for this postoperative bleeding clinical trial in Providence, RI

Secure & Confidential

Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Providence

    Convenient for RI 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 Providence site if eligible
  4. 4Begin participation

About This Postoperative Bleeding Study in Providence

The purpose of this study is to determine if applying a single dose of topical estrogen cream in the operating room at the end of your hysterectomy (removal of uterus and cervix) improves the postoperative experience with bleeding and potential symptoms of dysphoria (a feeling of discomfort or distress). Topical estrogen cream is sometimes used if patients have increased risk of bleeding with surgery but is not currently utilized in a consistent way. This study aims to answer the question of whether this is a helpful treatment and should be included in standard postoperative care.

Sponsor: Women and Infants Hospital of Rhode Island

Who Can Participate

Inclusion Criteria

Gender diverse/transgender men
Age 18 or older
Have been on testosterone for at least 6 months with plan to undergo gender-affirming hysterectomy and are willing to be randomized to the use of topical estrogen postoperatively.
Have stable physical and mental health
No contraindications to estrogen therapy
Must be proficient in English or Spanish
Must have access to a device to receive text messages for study follow up
Must agree to allow their medical data to be used for research purposes

Exclusion Criteria

Under age 18
Have not been on testosterone for at least 6 months prior to planned hysterectomy
Known allergy to topical estrogen

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 Providence?

Yes, this clinical trial (NCT06969326) has an active research site in Providence, RI 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.

Postoperative Bleeding Treatment Options in Providence, RI

If you're searching for postoperative bleeding treatment options in Providence, RI, this clinical trial (NCT06969326) 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 Providence research site is actively enrolling participants for this clinical trial. You'll receive care from experienced postoperative bleeding 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 postoperative bleeding clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Providence, RI