A Comparison of Eleview Versus Hetastarch as Injectate for EMR

Completed · Phase 4

Conditions studied: Procedural Bleeding, Delayed Bleeding, Post-Polypectomy Syndrome, Post Procedural Complication

In brief

EMR is a technique used for the removal of flat or sessile neoplasms confined to the superficial layers of the GI tract using a snare. Injection-assisted EMR is commonly used during resections of larger flat lesions as it provides submucosal lift of polyps, adenomas, other gastrointestinal mucosal lesions or early-stage cancers prior to EMR. This has been found to minimize mechanical or electrocautery damage to the deep layers of the gastrointestinal tract wall as the injectate provides a "safety cushion" as such between the area to be removed and healthy mucosal tissue. Several solutions are used today for injecting lesions including saline, hyaluronic acid, and hydroxyethyl starch (Hetastarch). Saline solution has been found to dissipate within minutes, which may result in a lower quality lesion lift. Hyaluronic acid provides a longer lift, but is expensive and is not readily available in the U.S. A new injectate known as Eleview has been developed for use in gastrointestinal endoscopic procedures and recently approved by the FDA. This injectate boasts a cushion of excellent height and duration through the use of an oil-in-water emulsion. However, the initial cost of this material is quite high ($80 per 10 ml). Hetastarch, which is the current injectate used by Dr Rex, is a safe and considerably inexpensive solution that provides prolonged submucosal elevation and lowers procedure times. Our study will aim to compare Eleview to Hetastarch in the hopes of finding the ideal submucosal injectate. This trial will focus on polyps of size ≥11 mm removed by snare EMR technique. Patients with lesions deemed not suitable for EMR due to features suggestive of sub-mucosal invasion will not be included.

Key facts

Study ID

NCT03350217

Run by

Indiana University

People needed

160

Starts

2017-10-09

Expected to finish

2019-01-07

Last updated by the study team

2019-12-17

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• 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.

Where it is running

• Indiana University — Indianapolis, Indiana, United States

Full record on ClinicalTrials.gov

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