Thursday, March 13, 2014

Baylor Seeks Volunteers in Need of Colonoscopies



Researcher with Baylor Research Institute, an analysis arm of Baylor Scott & White Health, have opened up participation for a new medicinal trial that might determine whether a specific blood examination are able to identify colon cancer before it actually develops. Early outcome of the evaluation, which screens for cancer-related microRNA in a person’s blood, seemed like positive, as released in the Journal of the National Cancer Institute. On the platforms of those promising findings, investigators are actually planning 400 healthy and treatment-naïve digestive tract or rectal cancer clinically diagnosed participants to determine this non-invasive blood test.

Image source: http://www.veooz.com/news/dGz52aX.html
Directed by principal investigator Richard Boland, MD, of Baylor University Medical Center’s Division of Gastroenterology, the investigation explores whether or not the blood assessment (which identifies the cancer-related biomarker serum miR-21), executed in conjunction with regular colonoscopies, should detect sufferers at high risk for colorectal cancer.

Right now, colorectal cancer is the third-leading root cause of cancer-related deaths in the USA, in accordance with the American Cancer Society. Some of those patients diagnosed with colorectal cancers, half are clinically diagnosed at advanced stages. Fewer than 50 percent of Americans undergo assessment for colorectal cancer, typically through an ordinary colonoscopy treatment.

“Our objective is always to improve those sobering statistics and to make available more comfortable examining solutions,” Dr. Boland said. “We’re emphasized by the preliminary outcome and are optimistic that measuring levels of miR-21 in the blood can help identify not simply cancer tumors, but also cancer risks.”

To continue with the analysis, researcher have asked for 200 healthy volunteers (who are due for a colonoscopy) and 200 patients clinically determined as colon or rectal cancer who have not undergone chemotherapy or radiation. Upon enrollment in the study, the research coordinator will accumulate a blood sample prior to the colonoscopy technique for all participants.

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