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Cryotherapy for GAVE (GAVE Cryo)

Primary Purpose

GAVE - Gastric Antral Vascular Ectasia, Bleeding, Bleeding Gastric

Status
Suspended
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
cryotherapy
Sponsored by
H. Lee Moffitt Cancer Center and Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for GAVE - Gastric Antral Vascular Ectasia focused on measuring GAVE, cryotherapy, bleeding, stomach, gastric, EGD, endoscopy

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Have GAVE
  2. Have had treatment discussion with non-study team member (physician or GI advanced practice provider) of alternatives and have elected Cryotherapy
  3. Patients with signs of GI bleeding defined as hemoglobin drop > 2 grams/dL, need for PRBC transfusion or overt bleeding (melena, hematemesis, hematochezia)
  4. Patients undergoing EGD with Ablation for GAVE (treatment naïve, RFA, banding, APC failures)
  5. Patients who underwent their last ablation at least 4 weeks prior
  6. Platelet count > 40,000
  7. International normalized ratio (INR) < 1.5
  8. Age > 18 years and < 90 years

Exclusion Criteria:

  1. Age < 18 years OR > 90 years
  2. Inability to obtain consent
  3. Anticoagulants or anti-platelet agents use (excluding aspirin) within the last 7-10 days
  4. Platelet count < 40,000
  5. INR > 1.5

Sites / Locations

  • H. Lee Moffitt Cancer Center and Research Institute
  • Long Island Jewish Medical Center
  • Columbia University Medical Center-NYPH
  • University Hospitals
  • Cleveland Clinic Foundation of America
  • Geisinger Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Cryotherapy for GAVE

Arm Description

Subjects will undergo cryotherapy for GAVE

Outcomes

Primary Outcome Measures

Clinical success
defined by the absence of PRBC transfusions and clinical evidence of bleeding

Secondary Outcome Measures

Technical success
defined as the ability to treat > 75% of the endoscopic area
Endoscopic success
defined as resolution of > 75% of the visible GAVE endoscopic surface
Mean/total number of PRBC transfused
transfusion of packed red blood cells
Change in hemoglobin
change in the lab test hemoglobin in grams/deciLiter
Technical failure
defined as the need for additional ablative modalities to achieve the primary study outcome

Full Information

First Posted
February 15, 2021
Last Updated
March 1, 2023
Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Long Island Jewish Medical Center, Geisinger Clinic, Columbia University, University Hospitals Cleveland Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04760873
Brief Title
Cryotherapy for GAVE
Acronym
GAVE Cryo
Official Title
Gastric Antral Vascular Ectasia Treatment With Balloon Cryotherapy: A Multicenter Prospective Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Suspended
Why Stopped
Transferring trial to new institution and needs to be reviewed/approved before enrolling new participants.
Study Start Date
October 14, 2020 (Actual)
Primary Completion Date
August 12, 2024 (Anticipated)
Study Completion Date
August 12, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Long Island Jewish Medical Center, Geisinger Clinic, Columbia University, University Hospitals Cleveland Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Gastric antral vascular ectasia (GAVE) is a condition that can lead to blood loss in the gastrointestinal tract and low blood counts or anemia. 1,2 GAVE is commonly associated with liver disease, kidney disease and autoimmune immune problems, but can also be seen in patients without those problems. 2-4 It is common for GAVE to cause hospitalization of patients and significant blood transfusion requirements. Given these problems, effective treatment of GAVE is needed to reduce these potential problems. These treatments are performed by a gastroenterologist through a flexible endoscope most often with argon plasma coagulation (APC).5-7 APC is only partially successful at eradicating GAVE and often entails repeated endoscopic procedures. Therapy with APC can also cause ulceration at times resulting in acute bleeding. Cryoablation is an attractive alternative to APC as it should not cause increased blood loss and case reports suggest that ablation may be achieved with limited number of endoscopic sessions. Prior problems with endoscopic cryotherapy include the high flow of gas and risk of perforation.8,9 A recent retrospective investigation by this group has evaluated the first generation cryotherapy balloon, demonstrating clinical safety and efficacy for GAVE.10 A new balloon cryotherapy spray device was recently developed and does not require venting. In this study we plan to prospectively evaluate the use of balloon cryotherapy to treat GAVE. We predict that the therapeutic response of balloon cryotherapy will be greater than 80% effective at achieving clinical success or the loss of overt bleeding and need for packed red blood cell (PRBC) transfusion at 6 months after treatment.
Detailed Description
Gastric antral vascular ectasia (GAVE), classically termed "watermelon stomach," is a condition of chronic acute blood loss in the gastrointestinal (GI) tract and can lead to common utilization of packed red blood cell (PRBC) transfusion. This condition occurs in 0.3% of endoscopic studies and 4% of studies performed for chronic or acute blood loss anemia.1,2 GAVE is commonly associated with autoimmune disease in 60% of cases and chronic liver disease in 30% of cases.2-4 Given the association with chronic liver disease, GAVE can be mistaken for other GI pathologies such as portal hypertensive gastropathy (PHG).11,12 Therefore, identification of GAVE is important in the management of this condition. Historically there have been 1 series highlighting the use of a monopolar probe and heater probe to treat GAVE. As these therapies have a low depth of thermal penetration, these therapies are not commonly utilized for GAVE.13,14 The most commonly implemented endoscopic therapy is argon plasma coagulation (APC). Among the largest studies of APC, the efficacy for treatment of GAVE is variable5,6 Additional outcomes include a reduction in the number of PRBC transfused in patients with GAVE that were treated with APC.7 In addition to APC, radiofrequency ablation (RFA) has also been evaluated in the setting of GAVE, leading to a decrease in the transfusions needed during follow-up.15 Similarly, cryotherapy using a spray catheter has been evaluated for GAVE.8,9 In these studies, the patients did demonstrate endoscopic improvement, lower transfusion requirements, and normalization of their hemoglobin. Despite, these results, the spray cryotherapy device requires the use of a venting tube to prevent complications and carries with it technical limitations that can make ablation difficult. Our study group, which includes University Hospitals, Case Western Reserve, Long Island Jewish Medical Center, Geisinger Medical Center, Columbia University Medical Center and The Cleveland Clinic Foundation of America This group has recently evaluated the first generation balloon cryotherapy device for GAVE, demonstrating efficacy and safety.10 Therefore, in this study we set out to prospectively evaluate the efficacy of a new balloon cryotherapy device for the treatment of GAVE. We predict that balloon cryotherapy will lead to greater than 80% clinical success (need for PRBC transfusion and absent overt bleeding).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
GAVE - Gastric Antral Vascular Ectasia, Bleeding, Bleeding Gastric
Keywords
GAVE, cryotherapy, bleeding, stomach, gastric, EGD, endoscopy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Subjects with GAVE will undergo therapy with a cryotherapy device
Masking
None (Open Label)
Allocation
N/A
Enrollment
69 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Cryotherapy for GAVE
Arm Type
Experimental
Arm Description
Subjects will undergo cryotherapy for GAVE
Intervention Type
Device
Intervention Name(s)
cryotherapy
Intervention Description
cryotherapy is a freeze spray that will be applied to GAVE for bleeding
Primary Outcome Measure Information:
Title
Clinical success
Description
defined by the absence of PRBC transfusions and clinical evidence of bleeding
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Technical success
Description
defined as the ability to treat > 75% of the endoscopic area
Time Frame
6 months
Title
Endoscopic success
Description
defined as resolution of > 75% of the visible GAVE endoscopic surface
Time Frame
6 months
Title
Mean/total number of PRBC transfused
Description
transfusion of packed red blood cells
Time Frame
6 months
Title
Change in hemoglobin
Description
change in the lab test hemoglobin in grams/deciLiter
Time Frame
6 months
Title
Technical failure
Description
defined as the need for additional ablative modalities to achieve the primary study outcome
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Have GAVE Have had treatment discussion with non-study team member (physician or GI advanced practice provider) of alternatives and have elected Cryotherapy Patients with signs of GI bleeding defined as hemoglobin drop > 2 grams/dL, need for PRBC transfusion or overt bleeding (melena, hematemesis, hematochezia) Patients undergoing EGD with Ablation for GAVE (treatment naïve, RFA, banding, APC failures) Patients who underwent their last ablation at least 4 weeks prior Platelet count > 40,000 International normalized ratio (INR) < 1.5 Age > 18 years and < 90 years Exclusion Criteria: Age < 18 years OR > 90 years Inability to obtain consent Anticoagulants or anti-platelet agents use (excluding aspirin) within the last 7-10 days Platelet count < 40,000 INR > 1.5
Facility Information:
Facility Name
H. Lee Moffitt Cancer Center and Research Institute
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States
Facility Name
Long Island Jewish Medical Center
City
New Hyde Park
State/Province
New York
ZIP/Postal Code
11040
Country
United States
Facility Name
Columbia University Medical Center-NYPH
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States
Facility Name
University Hospitals
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
Cleveland Clinic Foundation of America
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States
Facility Name
Geisinger Medical Center
City
Danville
State/Province
Pennsylvania
ZIP/Postal Code
17822
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Electronic health records database will allow for availability of demographic data and office-based follow-up records. ProVation MD software information will provide details regarding endoscopic parameters and intervention performed. Electronic records gathered for study purposes will only be available to study investigators and will be stored on an encrypted hard drive on a computer. Data will initially be entered with PHI attached so that all information can be obtained. Once all data collection is complete identifiers will be removed and random number assigned to the patients. Paper copies of study consents will be filled out in the endoscopy center and stored in a locked cabinet in the endoscopy center workroom. The door to the workroom with the cabinet is locked after hours and the endoscopy center is locked after hours as well.
Citations:
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Citation
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Results Reference
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