Colorectal Cancer Clinical Trial
Official title:
Clinical Trial Comparing Carnoy's and GEWF Solutions for Lymph Node Clearing Technique in Colorectal Cancer
NCT number | NCT02704988 |
Other study ID # | HMV-CRC1 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2015 |
Est. completion date | January 2019 |
Verified date | March 2019 |
Source | Hospital Moinhos de Vento |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Regional lymph node metastasis is a major determinant of local recurrence and overall survival rates in patients with colorectal cancer. Because of the poor prognosis associated with the presence of lymph node metastasis, stage III colorectal cancer patients should receive adjuvant treatment with chemo and / or radiation therapy according to the site of tumor. Several authors have investigated the use of revealing solutions for lymph node clearance in colorectal cancer. Most studies comparing conventional histopathological specimen examination to any lymph node clearing technique showed that the use of revealing solutions increases the mean number of lymph nodes harvested, usually in a statistically significant manner. It is still controversial the impact of the use of revealing solutions for upstaging of lymph node status and consequently for the indication for adjuvant therapy. Therefore will be conducted a randomized clinical trial to compares the performance of GEWF and Carnoy solutions for the histopathological examination of patients with colorectal cancer. The aim of this study is to determine the lymph node revealing solution with the best performance (increase in the mean number of lymph node harvested and lymph node upstaging) in patients with colorectal cancer.
Status | Completed |
Enrollment | 181 |
Est. completion date | January 2019 |
Est. primary completion date | June 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Histologically proven colorectal adenocarcinoma - Voluntary agreement of the patient to participate in research - Voluntary agreement of the surgeon to participate in research Exclusion Criteria: - Absence of accurate histopathological data - Unplanned extended resection - Synchronous colorectal cancer - Inflammatory bowel disease - Extended lymphadenectomy |
Country | Name | City | State |
---|---|---|---|
Brazil | Hospital Moinhos de Vento | Porto Alegre | Rio Grande Do Sul |
Lead Sponsor | Collaborator |
---|---|
Hospital Moinhos de Vento |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Increased lymph node sample | Additional number (unit measure) of lymph nodes identified by the lymph node clearing technique (visual and manual examination with Carnoy's or GEWF solutions) compared to the initial number (unit measure) of lymph nodes identified by the conventional technique (visual and manual examination with formaldehyde). | 1 week | |
Secondary | Additional lymph node metastases | Presence of metastases in the additional lymph nodes harvested | 1 week | |
Secondary | Change of lymph node staging | Increase of lymph node staging status (migration from N classification to higher staging), according to the 7th edition of the American Joint Committee on Cancer, with the lymph node clearing technique (visual and manual examination with Carnoy's or GEWF solutions) compared to the initial lymph node staging by the conventional technique (visual and manual examination with formaldehyde). | 1 week | |
Secondary | Indication for adjuvant treatment | Patient (unit measure) who had indication for adjuvant treatment (chemotherapy, radiotherapy or combined chemoradiotharepy) to treat colorectal cancer due to the outcome changes of the lymph node staging after using the lymph node clearing technique (visual and manual examination with Carnoy's or GEWF solutions). | 1 month |
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