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Full-thickness Laparo-endoscopic Excision vs Laparoscopic Colectomy for Colonic Tumors

Not Applicable
Conditions
Colorectal Neoplasms, Benign
Interventions
Procedure: laparoscopic colon resection
Procedure: full-thickness laparo-endoscopic colon adenomas excision
Registration Number
NCT04801355
Lead Sponsor
State Scientific Centre of Coloproctology, Russian Federation
Brief Summary

Adenoma - carcinoma is a classic pathway of carcinogenesis. On this basis, timely removal of colon adenomas is a prophylactic measure to prevent colon cancer.

The standard treatment of colorectal adenomas is endoscopic mucosal resection or submucosal dissection (ESD). In 10 - 15% of cases the ESD is impossible, due to the size of the tumor, inconvenient localisation in the area of the diverticulum or appendix, the presence of fibrosis in the submucosal layer (Currie AC framework IDEAL // Colorectal Disease. 2019. No. 9 (21). P. 1004-1016.), (Suzuki S. Short-term results of laparoscopic endoscopic cooperative surgery of colorectal tumors (LECS-CR) in cases of endoscopically inoperable colorectal tumors // Surgery today . 2019. No. 12 (49). S. 1051-1057.). In that cases the segmental colectomy is justified.

An alternative to colectomy is a hybrid laparo-endoscopic surgery, which reduce postoperative hospital stay, incidence of complications and provide a comparable level of radicality (Lee SW, Garrett KA, Milsom JW Combined endoscopic and laparoscopic surgery (CELS) // Seminars on surgery of the colon and rectum. 2017. No. 1 (28). S. 24-29).

Thus, the planned study will contribute to the introduction into practice of an alternative method of management with tumors of the colon without signs of invasive growth when the endoscopically removal is impossible.

Detailed Description

During the study we will recruit the patients with colon epithelial tumors without signs of invasive growth which that cannot be removed endoscopically. In case of high risk of conversion endoscopic procedure the patient will be discussed on MD consillium. All of them will be informed about the possibility of resection methods in the absence of using endoscopic technics. Then the patients will be prepared for the operation in accordance with the method adopted in the clinic. At first colonoscopy will be performed in the operating room. Those patients for whom to perform endoscopic removal of the formation is impossible will be randomized intraoperatively using an Internet resource into 2 groups (main and comparison group).

The patients of the main group will undergo to hybrid laparo-endoscopic operation and comparative group - to laparoscopic colon resection.

After surgical procedure a pathomorphological examination of the speciments will performed with assessment of its quality. Postoperative complications in both groups will be recorded in accordance with the Clavien-Dindo classification. The level of postoperative pain will also be registred according to the visual analogue pain scale (VAS). Also we will be study the time of activation of patients, patient self-care scope according to the Bartell scale, postoperative hospital stay will be assessed.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
100
Inclusion Criteria
  1. Patients age is 18 years and older
  2. Patients with colonic epithelial neoplasms without signs of invasive growth and not removable endoscopically
  3. Informed agreement
Exclusion Criteria
  1. Positive regional lymph nodes
  2. FAP
  3. The presence of an intestinal stoma
  4. ASI > III
  5. Patients with IBD
  6. Refusal of the patient to participate in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
laparoscopic resectionlaparoscopic colon resectionpatients with colonic adenomas who will undergo to laparoscopic segmental resection
full-thickness laparo-endoscopic colon adenomas excisionfull-thickness laparo-endoscopic colon adenomas excisionpatients with colonic adenomas who will undergo to laparo-endoscopic full-thickness colon resection
Primary Outcome Measures
NameTimeMethod
R1 resection rate30 days

In according to pathological examination

Secondary Outcome Measures
NameTimeMethod
The level of postoperative pain10 days

The level of postoperative pain with using a visual analogue pain scale: The patient assesses the postoperative pain from 0 to 10 points (0 points - no pain, 10 - unbearable pain).

The incidence and structure of postoperative complications30 days

The incidence and structure of postoperative complications according to the Clavien-Dindo scale (I-grade - any deviation from the normal course of the postoperative course without the need for pharmacological, surgical, endoscopic or interventional radiological interventions. drugs that are acceptable include antiemetics, antipyretics, analgesics, diuretics, and electrolytes. In addition, this grade includes a wound infection "stopped at the patient's bedside", V grades - Death of the patient)

Trial Locations

Locations (1)

Ryzhikh National Medical Research Center of Coloproctology, Moscow, Russian Federation

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Moscow, Russian Federation

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