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NCT Number: NCT07361016

Comparison of Laparoscopic and Open Total Mesocolic Excision With Central Vascular Ligation for Right Colon Carcinoma

The goal of this observational comparative study is to assess whether laparoscopic complete mesocolic excision with central vascular ligation (L-CME with CVL) provides improved short-term surgical outcomes compared with open complete mesocolic excision with central vascular ligation (O-CME with CVL) in patients with right-sided colon cancer.

The primary questions this study aims to answer are:

Does laparoscopic CME with CVL reduce blood loss, postoperative complications, and length of hospital stay compared with open CME?

Does laparoscopic CME with CVL achieve equivalent surgical specimen quality and short-term oncological outcomes compared to the open approach?

Researchers compared laparoscopic versus open right hemicolectomy with CME and CVL in adult patients diagnosed with right colon cancer who were eligible for elective surgical resection.

Participants underwent standard preoperative assessment, including clinical evaluation, laboratory testing, imaging studies, colonoscopy, and biopsy confirmation. Surgical treatment consisted of either laparoscopic or open complete mesocolic excision with central vascular ligation, performed according to standardized oncologic surgical principles. Postoperative care followed an enhanced recovery protocol.

Primary outcome measures included operative time, intraoperative blood loss, time to first flatus, postoperative complications, and duration of hospital stay. Secondary outcomes included quality of the surgical specimen (lymph node yield, mesocolic integrity, and margin status) and short-term oncologic outcomes, including early recurrence during follow-up.

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Key information

Age range

25 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • rt cancer colon

Exclusion criteria

  • metastatisis

Treatment and study plan

right hemicolectomy laparoscopic surgery

Procedure

Laparoscopic right hemicolectomy or extended right hemicolectomy using complete mesocolic excision with central vascular ligation, pneumoperitoneum 12-14 mmHg via umbilical port, diamond-shaped port placement, medial-to-lateral dissection along embryological planes, ligation of ileocolic (and right colic/middle colic branch when indicated) at origin, intra- or extracorporeal stapled ileotransverse anastomosis, specimen extraction through Pfannenstiel or right subcostal incision, standard perioperative care.

open rt hemicolectmy

Procedure

Open right hemicolectomy or extended right hemicolectomy using complete mesocolic excision with central vascular ligation, via midline laparotomy, lateral-to-medial mobilization, ligation of ileocolic (and right colic/middle colic branch when indicated) at origin, extracorporeal ileotransverse anastomosis with hand-sewn sutures, standard perioperative care.

Primary outcomes

  1. Length of Postoperative Hospital Stay

    Time frame: From surgery until discharge (up to 30 days)

    Number of days from the date of surgery to the date of hospital discharge.

  2. Overall Postoperative Morbidity ( Incidence of postoperative complications)

    Time frame: Up to 30 days after surgery

    Occurrence of any postoperative complication, including wound infection, anastomotic leak, abdominal collection, pulmonary infection, urinary tract infection, or deep vein thrombosis, occurring within the early postoperative period.

  3. Intraoperative Blood Loss ( Estimated blood loss (milliliters))

    Time frame: During surgery

    Volume of blood lost during surgical resection, measured intraoperatively.

  4. Operative Time ( Duration of surgery (minutes))

    Time frame: During surgery

    Time from skin incision to skin closure.

  5. Postoperative Recovery of Bowel Function (Time to first passage of flatus (hours))

    Time frame: Up to 72 hours postoperatively

    Time elapsed from completion of surgery to first postoperative flatus, indicating recovery of gastrointestinal motility.

Study contacts

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

Mohamed Gohar, assistant lecturer

CONTACT

[email protected]

01007664482

Sponsors and collaborators

Lead sponsor

Kafrelsheikh University

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Jan 22, 2026
Registry last updated
Jan 22, 2026

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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