LIRRH Trial for the Right-sided Colon Cancer (NCT07207317) | Clinical Trial Compass
RecruitingNot Applicable
LIRRH Trial for the Right-sided Colon Cancer
China120 participantsStarted 2025-05-01
Plain-language summary
The aim of this clinical trial is to compare the short- and long-term outcomes of laparoscopic ileocecal reconstruction right hemicolectomy (LIRRH) with those of traditional laparoscopic right hemicolectomy (TRH) for ascending and proximal transverse colon cancer.
Who can participate
Age range18 Years – 75 Years
SexALL
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Inclusion Criteria:
* Age 18-75 years
* ASA physical status ≤ III
* Endoscopy and biopsy-proven colon adenocarcinoma
* Contrast-enhanced abdominal CT showing primary tumor located in the ascending colon or proximal transverse colon (proximal one-third)
* Pre-operative clinical stage: TanyNanyM0
* Able to understand the study protocol, willing to participate, and provide written informed consent
Exclusion Criteria:
* History of hypertensive crisis or hypertensive encephalopathy.
* Severe cardiopulmonary insufficiency or any other contraindication to surgery.
* Uncorrectable electrolyte disturbances (e.g., potassium, calcium, magnesium).
* Evidence of significant bleeding diathesis or high hemorrhagic risk:
* Prior intracranial or intraspinal hemorrhage.
* Tumor invading major vessels with obvious bleeding risk.
* Thrombotic or embolic event within 6 months before study treatment, or significant vascular disease (e.g., surgical-repair aortic aneurysm).
* Clinically relevant hemoptysis or tumor bleeding of any cause within 1 month before screening.
* Therapeutic-dose anticoagulation within 2 weeks before study treatment (except low-molecular-weight heparin).
* Antiplatelet therapy within 10 days before study treatment (e.g., aspirin \> 325 mg/day, clopidogrel \> 75 mg/day, dipyridamole, ticlopidine, cilostazol).
* Active tuberculosis.
* Any active autoimmune disease or history of autoimmune disease with expected recurrence (including but not limited to SLE, RA, autoimmune hep…
What they're measuring
1
3-year disease-free survival (DFS)
Timeframe: From date of randomization until the date of first documented recurrence or death from any cause, assessed up to 36 months