A Comparison of Eleview Versus Hetastarch as Injectate for EMR

Injectate randomization:

Study patients will be randomly assigned to the Eleview or the Hetastarch treatment group in a 1:1 ratio. Randomization will occur at the site using envelopes provided by the Investigator. The envelope's contents will specify the treatment assignment for each patient and opened by the research team (PI will be blinded). The investigators will monitor the safety and effectiveness data. The appropriate solutions will be injected into the submucosal space beneath the lesion(s) to be excised before the lesion(s) is/are removed. Subjects in both groups will receive the appropriate volume of injectate deemed necessary by the PI for the individual patient.

Sample size and Statistical Analysis At least 200 patients will be enrolled. 100 of these patients will be randomized to Eleview injectate and 100 will be given the standard of care, Hetastarch injectate only. Efficacy and safety of Eleview injectate has only been reviewed in one previous study. Therefore, the planned sample size was not calculated using a statistical power analysis, but was regarded as sufficient to repeat the objectives of the COSMO study (2017) and satisfy the exploratory purposes of the present study.

Study personnel will carry out a simple randomization using a commonly used online generator. Randomization assignments will then be sealed until day of procedure until patient eligibility has been confirmed. The Principal Investigator will remain blinded and will perform all data analysis after completion of the study.

Data will be summarized and compared using classic descriptive statistics, i.e. mean, standard deviation, coefficient of variation (%), minimum, median and maximum values for quantitative variables, and frequencies for qualitative variables.

The Sydney Resection Quotient will be compared between treatment groups using a Wilcoxon Rank-Sum test. The proportion of subjects with en bloc resection of all endoscopically visible lesions will also be compared between treatment groups using a Fisher's exact test. A nominal alpha level of 0.05 will be used for both the comparisons.

No formal comparison will be performed for the secondary endpoints.

Inclusion criteria

• Sex and age: men and women > 18 years old
• Subjects referred for EMR of polyps of size ≥11 mm
• ASA score 1, 2 or 3.
• Contraception: Women of childbearing potential must have a negative pregnancy test (one is provided as the standard of care) or sign a waiver. Post-menopausal women must have been in that status for at least 1 year (per standard of care).
• Subject is willing and able to participate in the study procedures and to understand and sign the informed consent

Exclusion criteria

• Age: Subjects is under 18 years old
• Consent: Vulnerable subjects including those who are unable to consent
• Pregnancy: Pregnant or breastfeeding women
• ASA score <3
• Physical findings: Abnormal physical findings that may interfere with the study objectives
• Study participation: Subjects currently participating in another clinical study or previously enrolled in another clinical study in the last 30 days
• Excluded lesions:

• Lesions less than 11 mm in largest dimension
• Lesions involving the muscularis propria (T2 lesions)
• Ulcerated depressed lesions (Paris type III) or pathology proven invasive carcinoma
• Proven malignant disease locally advanced or with metastasis
• Active inflammatory bowel disease lesion, e.g ulcerative colitis, Crohn's disease
• Endoscopic appearance of invasive malignancy
• Previous partial resection or attempted resection of the lesion
• Allergy: Proven or potential allergic reaction to study products or history of anaphylaxis to drugs
• Severe liver disease.
• Known or suspected gastrointestinal obstruction or perforation, active diverticulitis, toxic megacolon,
• Inflammatory bowel disease e.g ulcerative colitis or Crohn's disease
• Hemostasis disorders (eg Von Willebrand disease, factor V Leiden thrombophilia or haemophilia), known clotting disorder (INR>1.5).
• Subject with any other current serious medical conditions that would increase the risks associated with taking part in the study.
• Patients must be advised to stop anticoagulation medications prior to the procedure per local practice guidelines and should re-start as clinically indicated after the procedure.