Phase
Condition
Neoplasms
Treatment
Endoscopic submucosal dissection (ESD)
Endoscopic mucosal resection (EMR)
Clinical Study ID
Ages 18-85 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults (at least 18 years old).
LSL-NG FE type ≥ 20mm or LST-G mixed type ≥30mm who have not been previously treatedor received submucosal injection, regardless of their location in the colon.
LSL-NG FE type ≥ 20mm or LST-G mixed type ≥30mm WITHOUT a demarcated area
The patient must have undergone a complete colonoscopy, reaching the cecum, todetect possible synchronous lesion. If this procedure has not been done previously,it will be performed prior to the inclusion of the patient in the study.
Patients able to fill in questionnaires written in Spanish or English.
Exclusion
Exclusion Criteria:
Contra-indication to colonoscopy.
Contra-indication to general anesthesia.
Inability to stop antiplatelet agents and anti-coagulant according to the EuropeanSociety of Gastro-Intestinal Endoscopy guidelines.
Patients with > 1 lesion meeting the inclusion criteria.
LSL-NG FE type ≥ 20mm or LST-G ≥30mm mixed type that have been previously treated (Recurrence or residual lesion after previous endoscopic or surgical treatment).
LSL-NG FE type ≥ 20mm or LST-G ≥30mm mixed type with previous submucosal injection,even if a resection attempt with a snare was not finally performed.
Lesions with suspicion of deep submucosal invasive carcinoma: depression or invasivepit-pattern (Vi within a demarcated area or Vn).
Submucosal mass like elevation within a LSL-NG FE type.
LSLs having a previous biopsy or tattooing. Previous biopsies of the lesion shouldonly be allowed if LSL-G mixed type > 30 mm and samples were taken out of the flatarea.
LSL-G with a Buddha like deformation (Polyp on polyp)
LSL involving a surgical anastomosis.
LSL involving the appendicular orifice.
LSL involving the terminal ileum.
Patient's refusal to participate in the study
Presence of inflammatory bowel disease
Pregnant or lactating women.
Hereditary colorectal cancer syndrome or hereditary polyposis.
Patient under legal protection and or deprived of liberty by judicial oradministrative decision.
Patient already participating in an interventional clinical research protocol
Patient who cannot be followed for the duration of the study.
Inability to sign the informed consent of the study.
Study Design
Study Description
Connect with a study center
Hospital Universitario "12 de Octubre"
Madrid, 28041
SpainActive - Recruiting
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