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Comparison of D2 vs D3 Lymph Node Dissection for Right Colon Cancer (RICON)

Comparison of D2 vs D3 Lymph Node Dissection for Right Colon Cancer (RICON)

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03200834
Enrollment
239
Registered
2017-06-27
Start date
2017-01-25
Completion date
2029-01-03
Last updated
2025-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colon Cancer

Keywords

Right colon cancer, D3 dissection, complete mesocolic excision, Hemicolectomy

Brief summary

Comparing different method of surgical technique D2 lymph node dissection vs D3 for right colon cancer.

Interventions

PROCEDURERight Hemicolectomy with D2 lymph node dissection

Remove right part of colon with lymph node dissection №201, №202, №211, №212 (if present), №221,№222 (Japanese classification).

PROCEDURERight Hemicolectomy with D3 lymph node dissection

Remove right part of colon with lymph node dissection №201, №202, № 203, №211, №212 (if present), №213 (if present) №221,№222, №223 (for hepatic flexure and proximal part of transverse colon cancer)(Japanese classification).

Sponsors

Donetsk National Medical University
CollaboratorOTHER
I.M. Sechenov First Moscow State Medical University
CollaboratorOTHER
G.V. Bondar Republican Cancer Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Agreement of the patient to participate in trial 2. Colon cancer (only adenocarcinoma ) 3. The tumor located between the cecum and the right 1/3 of transverse colon 4. Tumors T3,Т4а,b N0-2 (II-III stages) 5. Tolerance of chemotherapy 6. ECOG 0-2

Exclusion criteria

1. Patients with distant metastases 2. Tumors T1-2 (I stage) 3. Complications of tumor (perforation and full bowel obstruction) 4. Previous radiotherapy or chemotherapy 5. Synchronous or metachronous tumors 6. Women during Pregnancy or breast feeding period

Design outcomes

Primary

MeasureTime frameDescription
5-year survivalUp to 5 years post-operativedeath from any cause

Secondary

MeasureTime frameDescription
morbiditywithin the first 30 days after surgerypostoperative complications
mortalitywithin the first 30 days after surgerydeath after surgery
Disease free survival 5 years after initial surgeryUp to 5 years post-operativelocal and distant metastasis during 5 years after operation

Countries

Ukraine

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026