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NCT Number: NCT05807646

Reduced Dissemination of Tumor Cells With Primary Ligation of the Inferior Mesenteric Vein in Rectal Cancer Patients.

Effect of ligation sequence of the inferior mesenteric artery and vein on circulating tumor cells and survival in laparoscopic rectal cancer surgery: a prospective, multicenter, randomized controlled study (ARVECTS)

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Key information

About this study

Several studies have demonstrated that the presence of circulating tumor cells (CTCs) in the peripheral blood can be a surrogate biomarker to predict recurrence and prognosis of rectal cancer. CTCs are released from the primary tumor into the bloodstream and have the potential to spread to distant sites and develop into micro-metastatic deposits. Numerous studies have demonstrated that surgical manipulation could promote the dissemination of tumor cells into the circulation. Theoretically, the potential risk of tumor cell dissemination can theoretically be minimized if the effluent vein was ligated first. However, there is no regulation in the current guidelines on the sequence of ligation of the inferior mesenteric artery and vein during rectal cancer surgery owing to a lack of sufficient evidence. This multi-center randomized controlled trial is to investigate effect of ligation sequence of the inferior mesenteric artery and vein on circulating tumor cells and survival in laparoscopic rectal cancer surgery

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 18-75 years;
  • Histopathologically confirmed as rectal adenocarcinoma(tumor located within 15 cm from the anal verge at colonoscopy);
  • Patients with a stage I-III rectal cancer eligible for surgery and R0 resection is expected, patients with pelvic lateral lymph nodes metastasis are ineligible;
  • ECOG score: 0-1;
  • ASA score: I/II/III;
  • Laparoscopic surgery;
  • Informed consent.

Exclusion criteria

  • Patients who have received preoperative treatment (such as preoperative radiotherapy and chemotherapy);
  • Receiving transanal total mesorectal excision (taTME), specimen extraction through natural lumen (NOSES) ;
  • Recurrent rectal cancer;
  • Simultaneous or metachronous colorectal cancer;
  • Malignant tumors of other organs in the past 5 years or at the same time;
  • The results of preoperative physical examination and imaging examination showed that: (1) the tumor involved the surrounding organs and required combined organ resection; (2) distant metastasis; (3) could not be resected at R0;
  • Pregnant or lactating women;
  • Patients with severe mental disorder;
  • It is not suitable for patients undergoing laparoscopic surgery (such as extensive adhesion caused by previous abdominal surgery or inability to tolerate artificial pneumoperitoneum);
  • History of unstable angina pectoris or myocardial infarction in the past 6 months;
  • Have a history of cerebrovascular accident in the past 6 months;
  • Systemic administration of corticosteroids within 1 month before enrollment;
  • Taking folic acid related drugs within half a year before operation.
  • Severe cardiac insufficiency (FEV1<50% of predicted values);
  • Emergency surgery.

Treatment and study plan

Vein ligation first

Other

During this procedure, patients undergo laparoscopic rectal cancer surgery with the inferior mesenteric vein ligated first.

Artery ligation first

Other

During this procedure, patients undergo laparoscopic rectal cancer surgery with the inferior mesenteric artery ligated first.

Primary outcomes

  1. The changes of the level of circulating tumor cells in the peripheral blood

    Time frame: During the surgery

    The changes of the level of circulating tumor cells in the peripheral blood before cutting the skin and after closing the abdomen

Secondary outcomes

  1. 3-year disease-free survival

    Time frame: From date of surgery, assessed up to 36 months

    The proportion of patients with no disease recurrence and metastasis after 3 years of surgery

  2. 3-years overall survival

    Time frame: From date of surgery, assessed up to 36 months

    The proportion of patients who survived 3 years after surgery

  3. Recurrence pattern

    Time frame: From date of surgery, assessed up to 36 months

    Recurrence patterns are classified into five categories at the time of first diagnosis: locoregional, hematogenous, peritoneal, distant lymph node, and mixed type

  4. Blood loss

    Time frame: During the surgery

    Blood loss during the surgery

  5. Operation time

    Time frame: During the surgery

    Operation time

  6. Conversive rate

    Time frame: During the surgery

    Conversive rate

  7. Number of lymph nodes collected

    Time frame: During the surgery

    Number of lymph nodes collected

  8. Intraoperative morbidity and mortality rates

    Time frame: During the surgery

    The intraoperative morbidity rates are defined as the rates of event observed within operation

  9. Postoperative morbidity and motality rates

    Time frame: 30 days

    This is for the early postoperative complication, which defined as the event observed within 30 days after surgery

  10. Postoperative recovery course

    Time frame: 10 days

    Time to first ambulation, flatus, liquid diet and soft diet, duration of postoperative hospital stay and postoperative pain are used to assess the postoperative recovery course.Visual analog pain score method is used to evaluate the difference of postoperative pain degree

Study contacts

Contact information is provided by the study sponsor or research team.

Tao Pan, Doctor

CONTACT

[email protected]

+86-18181986821

Sponsors and collaborators

Lead sponsor

Sichuan Cancer Hospital and Research Institute

Other

Collaborators

  • Sichuan Provincial People's Hospital
  • The Second People's Hospital of Chengdu

Registry information

Official study title

Effect of Ligation Sequence of the Inferior Mesenteric Artery and Vein on Circulating Tumor Cells and Survival in Laparoscopic Rectal Cancer Surgery: a Prospective, Multicenter, Randomized Controlled Study (ARVECTS)

Important dates

Study start
2025
Primary completion
2025
Study completion
2028
First posted
Apr 11, 2023
Registry last updated
Feb 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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