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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05109130
Other study ID # GIHSYSU-20
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 18, 2021
Est. completion date October 18, 2025

Study information

Verified date April 2023
Source Sun Yat-sen University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The primary purpose of this study is to compare the changes of circulating tumor cells (CTCs) at different time points in rectal cancer patients undergoing laparoscopic or transanal endoscopic radical resection. Our secondary purpose is to explore the effects of perioperative circulating tumor cells on tumor recurrence and metastasis.


Description:

Mid-low rectal cancer is one of the common malignant tumors and the incidence has increased significantly in recent years. At present, surgery is still the most important and effective method for the treatment of mid-low rectal cancer. Traditional laparoscopic surgery and emerging transanal total mesorectal excision (TaTME) are the main methods. More than one-third of rectal cancer patients will eventually occur local recurrence and distant metastasis, which are the most important factors affecting prognosis. Circulating tumor cells may lead to distant metastasis, so the detection of CTCs in blood has important clinical significance in predicting the recurrence and metastasis of rectal cancer and monitoring treatment response. Due to the different degrees of contact between distinct surgical methods, this may lead to an increase in the quantity of CTCs in the blood, which may affect the prognosis of patients. Therefore, the investigators conducted a randomized controlled study to compare the changes in the quantity of CTCs in the central vein before, during and after operation in rectal cancer patients undergoing transanal endoscopic or laparoscopic radical resection. To explore the effect of two surgical methods on the risk of micrometastasis, and to provide evidence for the selection and improvement of rectal cancer treatment.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 100
Est. completion date October 18, 2025
Est. primary completion date October 25, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Mid-low rectal cancer. 2. Single lesion. 3. No metastasis. 4. Clinical Stage T2-3, N0-1. Exclusion Criteria: 1. History of malignant tumors. 2. Acute bowel obstruction, bleeding or perforation. 3. Received neoadjuvant treatment. 4. Tumor over 6cm in diameter or in severe adhesion with surrounded tissues. 5. Severe other contradictions of surgery. 6. Pregnant women will be excluded. Exit Criteria: 1. The patient suffered from massive hemorrhage. 2. The operation mode needs to be changed according to the patient's condition.

Study Design


Intervention

Procedure:
Surgical approach
Different surgical methods for rectal cancer resection

Locations

Country Name City State
China Department of colorectal surgery, the Sixth Affiliated Hospital, Sun Yat-Sen University Guangzhou Guangdong

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of circulating tumor cells during laparoscopic or transanal endoscopic surgery To determine the changes of circulating tumor cells in rectal cancer patients undergoing laparoscopic or transanal endoscopic radical resection before operation and 5 days after operation. 1 years
Secondary Disease free survival Determine relationship of CTC numbers and local recurrence and distant metastasis 3 years
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