Salt Lake City, UTNCT06665945Now EnrollingIRB Ready

Ovarian Cancer Clinical Trial in Salt Lake City, UT

Access cutting-edge ovarian cancer treatment through this clinical trial at a research site in Salt Lake City. Study-provided care at no cost to qualified participants.

Sponsored by University of Utah

Quick Self-Assessment

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Expert Care in Salt Lake City

Access ovarian cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related ovarian cancer treatment provided free

Apply for This Salt Lake City Location

Check if you qualify for this ovarian cancer clinical trial in Salt Lake City, UT

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

Why Participate?

  • No-Cost Study Care

  • Local to Salt Lake City

    Convenient for UT 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 Salt Lake City site if eligible
  4. 4Begin participation

About This Ovarian Cancer Study in Salt Lake City

The purpose of the SENTRY (Stability Enhanced Transcriptional Analytics) Study is to test whether combining a unique analytical approach with changes in platelet RNA expression accurately diagnoses ovarian cancer. Using retrospective data, the investigators have developed an approach that appears to accurately classify ovarian cancer with relatively high sensitivity and specificity. The SENTRY Study will build upon these retrospective analyses to prospectively recruit women with ovarian cancer or an ovarian mass (and healthy control women), obtain platelet RNA samples from whole blood, and perform validation analyses to test our hypothesis.

Sponsor: University of Utah

Who Can Participate

Inclusion Criteria

Women aged 21 years or older
Diagnosed with any type of ovarian or pelvic mass
Treatment naïve for current ovarian cancer (if cancer has been diagnosed)
The treating medical provider(s) are planning to perform a biopsy, surgery, or other diagnostic procedure to further evaluate the ovarian or pelvic mass (if not already diagnosed prior to consent)

Exclusion Criteria

Any other active malignancy
Other diagnosis of any cancer within the last 6 months except for non-melanoma skin cancer or carcinoma in situ of the cervix
Treatment for any cancer within the last 6 months except for non-melanoma skin cancer or carcinoma in situ of the cervix. Adjuvant endocrine therapy or other maintenance therapy is allowed.
Currently receiving chemotherapy, radiation therapy, or other treatments for ovarian cancer
Has already undergone complete ovarian mass resection
Unable to provide blood sample Study Population 3: Control Women without Ovarian Cancer (n=30) Inclusion Criteria: 1\. Women aged 21 years or older Exclusion Criteria:
Any active malignancy or diagnosis of cancer within the last 6 months except for non-melanoma skin cancer or carcinoma in situ of the cervix
Treatment for any cancer within the last 6 months except for non-melanoma skin cancer or carcinoma in situ of the cervix
Hospitalization or surgery (other than minor surgery such as mole removal) within the last 8 weeks
Renal failure (defined as eGFR \< 60 mL/min/1.73m² or on dialysis)
Liver failure (defined as having hepatic encephalopathy of any degree, OR moderately severe coagulopathy defined as INR ≥ 1.5, OR known cirrhosis, OR ALT of ≥ 10X ULN, OR total bilirubin of ≥ 3.0 mg/dL, OR diagnosis of liver failure)
Decompensated or end-stage heart failure (defined as ACC/AHA Stage C or Stage D heart failure)
Poorly controlled diabetes mellitus (defined as a HbA1c \> 9.0%)
Venous thrombosis, myocardial infarction, or stroke within the last 8 weeks
Currently pregnant or have been pregnant within the last 12 weeks
Any blood product transfusion within the last 8 weeks
Personal history of ovarian cancer at any time
History of bilateral salpingo-oophorectomy
History of oophorectomy
Unable to provide blood sample

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 Salt Lake City?

Yes, this clinical trial (NCT06665945) has an active research site in Salt Lake City, UT 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.

Ovarian Cancer Treatment Options in Salt Lake City, UT

If you're searching for ovarian cancer treatment options in Salt Lake City, UT, this clinical trial (NCT06665945) 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 Salt Lake City research site is actively enrolling participants for this clinical trial. You'll receive care from experienced ovarian cancer 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 ovarian cancer clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Salt Lake City, UT