Study of CryoSpray Ablation of Low Grade or High Grade Dysplasia Within Barrett's Esophagus (ICE)

CSA Medical

Status and phase

Terminated

Phase 4

Conditions

High Grade Dysplasia

Low Grade Dysplasia

Barrett's Esophagus

Treatments

Device: CryoSpray Ablation System (510(k) NO: K070893)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00526786

16-00016-00

Details and patient eligibility

About

The purpose of this study is to evaluate the safety and effectiveness of the CryoSpray Ablation System to treat esophageal low grade dysplasia (LGD) or high grade dysplasia (HGD) within Barrett's Esophagus (BE).

Full description

The study will consist of an estimated 200 subjects with HGD or LGD within BE who are deemed inoperable or refuse standard surgical treatment. A maximum of 20 investigational sites will participate with a maximum of ten subjects per site.

Enrollment

78 patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Karnofsky performance status of 50-100%
Life expectancy greater than 5 years
Hematopoietic, Hepatic and Renal lab clearance
Previous endoscopy with histological confirmation of LGD or HGD within BE
For Group 2, deemed inoperable based on the following criteria: co-morbid conditions such as severe heart, lung, kidney or liver disease; or refusal of surgical intervention after a thorough unbiased discussion of surgery.
For Group 2, endoscopic ultrasound (EUS) evaluation demonstrating no evidence of invasion or metastatic lymph node involvement (T0N0M0 by EUS).

Exclusion criteria

Pregnant, not practicing adequate contraception, intending to become pregnant, or lactating at any time during the study (approximately 2 years).
Esophageal stricture preventing passage of endoscope or catheter.
Active esophagitis
EMR performed less than 8 weeks prior to CSA treatment.
EMR performed on greater than 90% circumference of any area of the esophagus.
Any previous esophageal surgery, except fundoplication without complications.
Known history of unresolved drug or alcohol dependency that would limit ability to comprehend or follow instructions related to informed consent, post-treatment instructions, or follow-up guidelines.
Concurrent enrollment in an investigational drug or device trial that clinically interferes with the LCS Dysplasia endpoints.
Psychiatric or other illness deemed by the investigator as an inability to comply with this protocol.
Medically unfit or other contraindication to tolerate upper endoscopy.
Inability to tolerate therapy with a proton pump inhibitor (PPI).
Refusal or inability to give consent.
Other active malignancy (except nonmelanoma skin cancer or another cancer for which patient is deemed disease-free).
Concurrent chemotherapy.
Prior radiation therapy which involved the esophagus.
Prior adenocarcinoma involving the esophagus or stomach.
Prior or concurrent ablation therapy including, but not limited to, photodynamic therapy, multipolar electro coagulation, argon plasma coagulation, laser treatment, radio frequency, etc.