Sacramento, CANCT05321134Now EnrollingIRB Ready

Colo-rectal Cancer Clinical Trial in Sacramento, CA

Access cutting-edge colo-rectal cancer treatment through this clinical trial at a research site in Sacramento. Study-provided care at no cost to qualified participants.

Sponsored by University of California, Davis

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Expert Care in Sacramento

Access colo-rectal cancer specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related colo-rectal cancer treatment provided free

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Check if you qualify for this colo-rectal cancer clinical trial in Sacramento, CA

Secure & Confidential

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

Why Participate?

  • No-Cost Study Care

  • Local to Sacramento

    Convenient for CA 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 Sacramento site if eligible
  4. 4Begin participation

About This Colo-rectal Cancer Study in Sacramento

Currently a multiport robotic surgery platform (Intuitive Xi) is widely available and used for colorectal surgery indications. A Single port platform (Intuitive SP) is FDA approved for Head and Neck and Urology but has not been widely used in colorectal surgery. This study seeks to evaluate the safe and effective use of the SP platform for colorectal surgery indications.

Sponsor: University of California, Davis

Who Can Participate

Inclusion Criteria

The subject is male or female, greater than or equal to 18 years of age. If female, the subject has a negative urine pregnancy test and is not lactating, or has not been of childbearing potential for at least 3 months prior to use of study product. To be considered to be not of childbearing potential, the subject must be postmenopausal for at least 2 years; have had a hysterectomy or bilateral tubal ligation, or be proven to be otherwise incapable of pregnancy. If of childbearing potential, the subject must have been practicing one of the following methods of contraception consistently for at least 1 month prior to study entry and agree to continue practicing it during the study: hormonal contraceptives, intrauterine device, spermicide and barrier, spouse/partner sterility; or is practicing abstinence and agrees to continue abstinence or to start an acceptable method of contraception from the above list if sexual activity commences.
There is documentation of a colorectal diagnosis requiring operative interventions with clinical plans for a robotic operation.
For robotic transanal procedures, patients who would meet standard guidelines for a transanal procedures (T1N0 rectal adenocarcinoma, Precancerous adenomas, and localized neuroendocrine tumors) distal to 15 cm from the anal verge.
The subject is in good general health as evidenced by medical history and physical examination
The subject is able and willing to provide written informed consent.
The subject agrees to comply with the requirements of the protocol and complete study measures.
The subject has stable residence and telephone.

Exclusion Criteria

The subject is child less than 18 years of age
The subject is a female who is pregnant or lactating
The subject falls under the American Society of Anesthesia Class IV (Patients with severe systemic disease that is a constant threat to life).
The subject falls under American Society of Anesthesia Class V (Moribund patients who is not expected to survive without the operation)
The subject has a history of clinically significant renal, hepatic, neurological, cardiac or chronic pulmonary disease that in the judgment of the investigator precludes participation.
The subject has advanced/ Stage IV cancer
The subject has received neo-adjuvant chemotherapy or radiation therapy
The subject requires an emergency operation.
The subject is unable to fully comprehend or consent to the study
The subject is unwilling to be available for follow-up assessments.

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 Sacramento?

Yes, this clinical trial (NCT05321134) has an active research site in Sacramento, CA 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.

Colo-rectal Cancer Treatment Options in Sacramento, CA

If you're searching for colo-rectal cancer treatment options in Sacramento, CA, this clinical trial (NCT05321134) 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 Sacramento research site is actively enrolling participants for this clinical trial. You'll receive care from experienced colo-rectal 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 colo-rectal cancer clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Sacramento, CA