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NCT Number: NCT04871399

Complete Mesocolic Excision in Comparison With Conventional Surgery for the Right Colon Cancer

An Italian randomized controlled trial parallel-group in patients with a malignant tumor of the right or proximal transverse colon requiring right hemicolectomy.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Ospedale della Misericordia, Grosseto, Arezzo, Italy

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About this study

This study aims to compare the Complete Mesocolic Excision With Central Vascular Ligation (CME+CVL) with the standard (non-CME) right hemicolectomy in patients with right or proximal transverse colon cancer stage II-IV(AJCC 8th edition) to determine the short and long term outcomes in terms of disease-free survival (DFS) as a primary endpoint, and safety, oncologic outcomes, quality of surgery and quality of life (QoL) as secondary endpoints.

Eligible patients will be randomized with a 1:1 ratio between CME + CVL vs standard non-CME right colectomy. The randomization sequence will be generated centrally by a computed algorithm and kept concealed to investigators.

The Right colectomy with CME + CVL includes the removal of the accessory lymphovascular supply at their origins by resecting the colon and mesocolon in an intact envelope of visceral peritoneum and mesenteric fascia. Despite the surgical approach and the type of procedure adopted, the operation should be strictly conducted following the general rules for colorectal oncologic resection, particularly as concerns proximal and distal margins length and lymph node retrieval.

All surgical approaches (open, laparoscopic, or robotic) will be allowed while the type of anastomosis performed and drain placement will be up to the surgeon's discretion.

Demographic, baseline, perioperative and postoperative characteristics will be analyzed as well.

The study expected to last six and a half years, of which one and a half years for recruiting 416 patients, 208 each arm, with five years of follow-up. Patients will be followed up at 1, 4, 12, 24, 36, and 60 months postoperatively.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • American Society of Anesthesiologists(ASA) grade I-III.
  • Right colon cancer (*The right-sided location of the cancer is defined as the location from the caecum up to the proximal third of the transverse colon), preoperative assessment of tumor stage T2-T4a, any N or T any N+ according to the National Comprehensive Cancer Network(NCCN) clinical practice guidelines in oncology: colon cancer version 2.2015); no distant metastasis.
  • Informed consent

Exclusion criteria

  • Age > 85 years old.
  • T1, N0
  • T4b, any N
  • BMI > 30.
  • Metastatic disease (Abdominal and chest CT scan will be mandatory to exclude distant metastasis.)
  • American Society of Anesthesiologists(ASA) grade IV.
  • History of cancer in recent 5 years.
  • Need for Emergency surgery.
  • Infectious disease requiring treatment.
  • Pregnancy.
  • Use of systemic steroids.
  • No history of familial adenomatous polyposis, ulcerative colitis or Crohn's disease.

Treatment and study plan

Conventional Right hemicolectomy (Non-CME)

Procedure

Transecting the Ileocolic Vein and Artery close to the Superior Mesenteric Vessels without clearing the superior mesenteric vein (SMV) from the adipose tissue. Transecting the Right Colic Vein and Artery and superior right colic vein (when present) peripherally. Transecting the Right branches of the Middle Colic Vein (MCV) and the Middle Colic Artery (MCA) peripherally, without clearing the main trunk of the MCV and the MCA. The Right Gastroepiploic Vein and artery are never transacted.

Right hemicolectomy with CME+CVL

Procedure

Separation of the visceral fascia from the parietal fascia by sharp dissection leaving intact mesocolon coverage. Transecting the supplying vessels at their origin from the main vessels, particularly:

  • The Ileocolic Vessels, The Right Colic Vessels,The superior right colic vein (when present), The Right branches of the Middle Colic Vein and of the Middle Colic Artery
  • The MCV and MCA at their origin in case of cancer of the hepatic flexure or of the proximal third of the transverse colon, as well as The Right Gastroepiploic Vessels at their origin from the gastrocolic trunk of Henle (GCTH) and the gastroduodenal artery.

The SMV should be cleared from all adipose tissue all along its anterior surface until its intrapancreatic entrance.

Primary outcomes

  1. Disease-free survival at 3 years

    Time frame: 3 Years.

    The length of time after surgery without any signs or symptoms of local or distant recurrence.

Secondary outcomes

  1. Safety-Operative time.

    Time frame: Intraoperative

    Total time from incision to skin closure expressed in minutes.

  2. Safety-Intraoperative blood loss.

    Time frame: Intraoperative

    Defined by the volume drained in cm2 into aspiration systems and weight of gauzes, calculated, subtracting the weight of the dry gauzes and volume of saline solution used for irrigation.

  3. Safety-Intraoperative blood transfusion.

    Time frame: Intraoperative

    Defined as the number of red blood cells, platelets, or plasma units transfused during the intraoperative time.

  4. Safety- Intraoperative Complications.

    Time frame: Intraoperative

    Defined as any deviation from the ideal intraoperative course occurring during the operative time, Using the Classification of Intraoperative Complications(CLASSIC).

  5. Early postoperative complications.

    Time frame: 30 postoperative days.

    Number of patients with any deviation from the normal postoperative course grading by The Clavien-Dindo classification.

  6. Late postoperative complications.

    Time frame: From the 31st postoperative days to the end of the study.

    The number of patients with any deviation from the normal postoperative course grading by The Clavien-Dindo classification.

  7. Safety- Length of stay.

    Time frame: 30 Days.

    Defined as the length of an inpatient episode of care, calculated from the day of operation to the first discharge and based on the number of nights spent in the hospital.

  8. Safety- Postoperative mortality rate.

    Time frame: 30 Days.

    The all-cause death rate, within 30 days after surgery in or out of the hospital.

  9. Overall Survival at 3 years

    Time frame: 3 Years.

    Defined as the time from random assignment to the date of death due to any cause.

  10. Overall Survival at 5 years.

    Time frame: 5 Years.

    Defined as the time from random assignment to the date of death due to any cause.

  11. Disease-free survival.

    Time frame: 5 Years.

    Defined as the length of time after Surgical treatment (CME+CVL or Conventional non-CME procedure) that the patient survives without any signs or symptoms of colon cancer.

  12. Other Oncologic outcomes.

    Time frame: 30 Days.

    The number of positive, negative, and total lymph nodes harvested, Quality of surgery specimen, quality of life by EORTC specific Questionnaires

Study contacts

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

Hogla Aridai Resendiz Aguilar, MD

CONTACT

[email protected]

00393512338942

Mario Solej, MD

CONTACT

[email protected]

00393388624939

Sponsors and collaborators

Lead sponsor

University of Turin, Italy

Other

Collaborators

  • Agnelli Hospital, Italy
  • Azienda Ospedaliera Universitaria Policlinico "G. Martino"
  • Candiolo Cancer Institute - IRCCS
  • European Institute of Oncology
  • Federico II University
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
  • Maggiore Bellaria Hospital, Bologna
  • Ospedale Policlinico San Martino
  • Ospedale della Misericordia
  • S. Andrea Hospital
  • University of Rome Tor Vergata
  • Università degli Studi di Ferrara

Registry information

Official study title

Complete Mesocolic Excision With Central Vascular Ligation in Comparison With Conventional Surgery for the Right Colon Cancer: An Italian Randomized Trial

Acronym: CoME-In

Important dates

Study start
2020
Primary completion
2027
Study completion
2027
First posted
May 4, 2021
Registry last updated
Nov 14, 2022

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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