Charleston, SCNCT07149207Now EnrollingIRB Ready

Squamous Cell Carcinoma Head and Neck Cancer (HNSCC) Clinical Trial in Charleston, SC

Access cutting-edge squamous cell carcinoma head and neck cancer (hnscc) treatment through this clinical trial at a research site in Charleston. Study-provided care at no cost to qualified participants.

Sponsored by Medical University of South Carolina

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Expert Care in Charleston

Access squamous cell carcinoma head and neck cancer (hnscc) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related squamous cell carcinoma head and neck cancer (hnscc) treatment provided free

Apply for This Charleston Location

Check if you qualify for this squamous cell carcinoma head and neck cancer (hnscc) clinical trial in Charleston, SC

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Why Participate?

  • No-Cost Study Care

  • Local to Charleston

    Convenient for SC 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 Charleston site if eligible
  4. 4Begin participation

About This Squamous Cell Carcinoma Head and Neck Cancer (HNSCC) Study in Charleston

This study is for adult patients with head and neck cancer who are at risk of recurrence. The purpose of this study is to evaluate whether the use of Indocyanine Green (ICG) dye allows for better identification of tumor tissue during surgical procedures. Participation will include standard of care visits along with administration of ICG dye and imaging during surgery. Participation in this study will last approximately 6 weeks.

Sponsor: Medical University of South Carolina

Who Can Participate

Inclusion Criteria

Adult subjects at least 18 years of age.
Subjects presenting with squamous cell carcinoma of mucosal origin and are at risk for recurrence.
Good operative candidate as determined by the treating physician and/or multidisciplinary team.
Subject capable of giving informed consent and participating in the process of consent.
A WOCBP must be willing and able to use highly effective contraception from the time of informed consent throughout the study period. Acceptable forms of birth control include hormonal contraceptives (such as birth control pills, skin patch, vaginal ring, injection, and/or implant), intrauterine devices (IUDs), and barrier devices (such as condoms, diaphragm, cervical cap, and sponge).

Exclusion Criteria

Pregnant or breastfeeding, or expecting to conceive within the projected duration of the study.
A WOCBP who has had a positive urine or serum pregnancy test at the time of screening unless:
they are menopausal defined by not having a menstrual cycle within the last 12 consecutive months or
they have had a hysterectomy.
Known allergy to iodides or shellfish.
Inadequate organ function at time of screening as defined below: a. Hepatic
Total bilirubin \>2 x Institutional Upper Limit of Normal (IULN). Participants with a history of Gilbert's disease must have total bilirubin \<3mg/dL.
AST (SGOT) and ALT (SPGT) \>3 x IULN.
Currently incarcerated individuals

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 Charleston?

Yes, this clinical trial (NCT07149207) has an active research site in Charleston, SC 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.

Squamous Cell Carcinoma Head and Neck Cancer (HNSCC) Treatment Options in Charleston, SC

If you're searching for squamous cell carcinoma head and neck cancer (hnscc) treatment options in Charleston, SC, this clinical trial (NCT07149207) 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 Charleston research site is actively enrolling participants for this clinical trial. You'll receive care from experienced squamous cell carcinoma head and neck cancer (hnscc) 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 squamous cell carcinoma head and neck cancer (hnscc) clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Charleston, SC