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Prospective Study of Oncologic Outcomes After Laparoscopic Modified Complete Mesocolic Excision for Non-metastatic Right Colon Cancer [PIONEER Study]

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Yonsei University

Status

Invitation-only

Conditions

Adenocarcinoma of the Colon

Treatments

Procedure: Laparoscopic modified complete mesocolic excision

Study type

Observational

Funder types

Other

Identifiers

NCT03992599
4-2018-1162

Details and patient eligibility

About

This study is a multi-institutional, prospective, observational study evaluation oncologic outcomes of laparoscopic modified complete mesocolic excision (mCME) on right-sided colon cancer.

The primary outcome of this study is 3 year disease-free survival. Secondary outcome measures include 3 year overall survival, incidence of surgical complications, completeness of mCME, and distribution of metastatic lymph nodes.

Full description

The present study aims to evaluate the oncological outcomes of laparoscopic mCME on right-sided colon cancer. The right side of the colon was defined as the colon from cecum up to the proximal half of the transverse colon. The number of patients needs to get a 90% power is 250. Patients will be enrolled at five leading centers in South Korea. A complete information leaflet will give to the patients during the first consultation, which will correspond to the enrollment day. The preoperative, intraoperative, and postoperative period will be in complete accordance with the usual care of the center. The baseline demographics and conditions, as well as the perioperative items and the postoperative occurrences, will be recorded through a prior designed case report form. The follow-up encompasses 13 postoperative consultations: 1month, 3 months, after that every 3 months until 36 months.

The primary outcome of this study is 3-year disease-free survival. Secondary outcome measures include 3-year overall survival, the incidence of surgical complications, completeness of mCME, and distribution of metastatic lymph nodes. Review of resected surgical specimens and the operative field after completion of lymph node dissection will be done based on photographs to assess the quality if surgery.

Enrollment

250 estimated patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

    1. Qualitative diagnosis: a pathological diagnosis of adenocarcinoma; the tumor located between the cecum and the right 1/2 of transverse colon
    1. Patients suitable for curative surgery older than 19 years old
    1. ASA grade I-III
    1. Patients without preoperative treatment
    1. Informed consent

Exclusion criteria

    1. Informed consent refusal
    1. Patients who need emergency operation; such as perforation, malignant colonic obstruction
    1. Preoperative imaging examination results show: distant metastasis
    1. Hereditary colon cancer
    1. History of any other malignant tumor in recent 5 years, except for cervical carcinoma in situ which has been cured, basal cell carcinoma or squamous cell carcinoma of skin;
    1. Simultaneous or simultaneous multiple primary colorectal cancer
    1. Women during Pregnancy or breast feeding period

Trial design

250 participants in 1 patient group

Laparoscopic modified central mesocolic excision
Description:
Patients receiving laparoscopic colectomy with the concept of modified complete mesocolic excision for right-sided colon cancer
Treatment:
Procedure: Laparoscopic modified complete mesocolic excision

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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