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ARAT for Reflux Disease After Peroral Endoscopic Myotomy in Patients With Achalasia

Study acronym: ARAT
StatusEnrolling by Invitation
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated April 25, 2025 (before its estimated July 1, 2026 completion). Its status may not reflect the trial's current state.

Record History

  1. Primary completion date: Nov 1, 2022 to Jul 1, 2026
    • Study completion date: Dec 1, 2022 to Dec 1, 2026
    • Site details revised
    v5
  2. Primary completion date: Jun 1, 2022 to Nov 1, 2022v4
  3. Primary completion date: Apr 1, 2021 to Jun 1, 2022
    • Study completion date: Dec 1, 2021 to Dec 1, 2022
    v3
  4. Primary completion date: Nov 1, 2019 to Apr 1, 2021
    • Study completion date: Dec 1, 2020 to Dec 1, 2021
    v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The peroral endoscopic myotomy for the treatment of achalasia is associated with a higher incidence of gastroesophageal reflux disease compared with Heller's myotomy. Remodeling of the esophagogastric junction with hybrid argon plasma could decrease the passage of gastric or gastroduodenal content into the esophagus.
Trial Details
NCT Number NCT04065516
Lead Sponsor Coordinación de Investigación en Salud, Mexico
Conditions
(from sponsor)		 Achalasia, Gastroesophageal Reflux
Related terms Esophageal Achalasia, Gastroesophageal Reflux
Enrollment 44 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov