Recruiting

Cryotherapy

Sponsor:

Mayo Clinic

Code:

NCT07169799

Conditions

Gastric Antral Vascular Ectasia

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

trūFreeze® Spray Cryotherapy System (STERIS Endoscopy)

Study Details

Brief summary:

The purpose of this study is to evaluate the impact of cryotherapy spray treatment for eradication of gastric antral vascular ectasia by measuring the change in hemoglobin levels and transfusion requirements in the first 6 months of cryotherapy treatment compared to the previous 6 months

Conditions

Gastric Antral Vascular Ectasia

Study ID

NCT07169799

Start date

Dec 22, 2026

Status verified date

Mar, 2026

Completion date

Dec 31, 2028

Anticipated

Primary completion date

Sep 30, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria

• Diagnosis of antral-predominant GAVE: Endoscopic confirmation of gastric-antral vascular ectasia affecting the antrum, without severe portal-hypertensive gastropathy. Sub-classify as nodular or non-nodular GAVE.

  • Age: ≥ 18 years at the time of consent.
  • Recent transfusion-dependent anemia

  • ≥ 1 packed-RBC transfusion for GAVE-related bleeding within the last 6 months to maintain hemoglobin (Hgb) > 8 g/dL (or > 7 g/dL if no coronary/vascular disease).
  • Standard-of-care transfusion thresholds:

  • If no coronary artery/vascular disease (CVD): transfuse 2 units when Hgb < 7 g/dL.
  • If CVD present: transfuse 2 units when Hgb < 8 g/dL.
  • After any transfusion, re-check Hgb within 1 week and repeat transfusion per the same criteria as needed.
  • Documented transfusion history:

o Medical records must show indication that each transfusion was for presumed GAVE-related bleeding.
  • Treatment status:

o Either treatment-naïve or ≤ 3 prior endoscopic ablation sessions for GAVE.
  • Baseline data availability: Participant records must include endoscopic treatment dates, hemoglobin values, and transfusion data for 6 months prior to enrollment (extension up to 9 months permitted if data unavailable). Required elements:

  • total number of transfusions,
  • total number of prior endoscopic treatments, and calculated change in hemoglobin from baseline: Δ Hgb = Hgb(T-6 mo) - Hgb(T0) \[extendable to Hgb(T-9 mo) if 6-month data are incomplete\]
  • Capacity to consent: Able and willing to provide written informed consent.

Exclusion Criteria

  • Other gastrointestinal pathology

o Active peptic-ulcer disease, inflammatory bowel disease, severe portal-hypertensive gastropathy, or untreated esophageal/gastric varices.
  • Coagulopathy

o Known bleeding disorder or acquired coagulopathy not attributable to GAVE.
  • Severe comorbidity / high procedural risk

  • Advanced heart failure, severe renal impairment, or any condition classified ASA IV or V.
  • Estimated life-expectancy < 6 months.
  • Karnofsky performance status ≤ 40.
  • Deemed unfit for endoscopic procedures by the treating physician.
  • Pregnancy / lactation:

o Pregnant or breastfeeding, or planning pregnancy within 6 months of consent.
  • Prior incompatible therapy

o Previous cryoballoon ablation for GAVE.
  • Ability to participate

  • Unable or unwilling to comply with the protocol or follow-up schedule.
  • Unable or unwilling to provide written informed consent.

Study Design

Enrollment

50 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

other: Prospective arm: Spray Cryotherapy

Subjects to receive baseline endoscopic confirmation/classification of GAVE, laboratory panels, and clinical indices. Once confirmed, subjects will undergo cryotherapy procedure schedule.

Interventions

trūFreeze® Spray Cryotherapy System (STERIS Endoscopy)

This treatment consists of performing a diagnostic EGD to identify GAVE lesions. A catheter advances through the therapeutic channel to treat target areas with cryotherapy.

Primary outcome measure

  • Evaluate the clinical benefit of truFreeze® spray-cryotherapy in patients with gastric-antral vascular ectasia. [ Time Frame: over 6 month period ]

Central Contacts and Locations

Central contacts

Locations

Mayo Clinic in Florida

Recruiting

Jacksonville, Florida, United States, 32224

Contacts

Principal Investigator:

Swathi Eluri, M.D.

More Information

Sponsor

Mayo Clinic

Last update posted

Apr 3, 2026

Last verified

Mar, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Mayo Clinic on 2026-04-03.