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NCT Number: NCT06955520

Vonaprazan Versus Esomeprazole for Healing of LA Grade B or Higher Esophagitis After POEM

Peroral Endoscopic Myotomy (POEM) is a well-established treatment for achalasia; however, it is frequently associated with gastroesophageal reflux disease (GERD), with many patients developing LA grade B or higher esophagitis. Proton pump inhibitors (PPIs) like Esomeprazole are the standard treatment, but Vonaprazan, a potassium-competitive acid blocker (P-CAB), offers superior acid suppression and may provide enhanced healing in post-POEM reflux esophagitis.

Primary Objective:

• To compare the healing rates of LA grade B or higher reflux esophagitis at 8 weeks in patients receiving Vonaprazan 20 mg versus Esomeprazole 40 mg.

Secondary Objectives

* To assess improvement in reflux symptoms using the GERD-Q score at 8 weeks. * To evaluate the incidence of adverse events in each treatment group.

Recruiting

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Asian Institute of Gastroenterology /Aig Hospitals

Hyderabad, Telangana, 500082, India

Location status: Recruiting

Location contact

Rajesh Goud Mr Maragoni, M.Pharm MBA

CONTACT

[email protected]

04023378888 ext. 301

ZAHEER DR NABI, MBBS MDDNB

CONTACT

[email protected]

04023378888 ext. 503

About this study

Study Type:

  • Randomized, Open-Label, Two-Arm, Non-Inferiority Trial

Randomization and Blinding:

  • Randomization: 1:1 ratio between Vonaprazan 20 mg and Esomeprazole 40 mg.
  • Stratification: Based on LA grade (B vs. C/D) at baseline.
  • Blinding: Open-label study, but outcome assessors will be blinded.

Study Timeline:

  • All post-POEM patients receive Esomeprazole 40 mg for 2 months.
  • PPI is discontinued for 1 month (to allow reflux esophagitis to develop if persistent GERD exists).
  • At 3 months post-POEM, patients with LA grade B or higher esophagitis (on follow-up endoscopy) are randomized to either Vonaprazan 20 mg or Esomeprazole 40 mg for 8 weeks.
  • At 8 weeks post-randomization (5 months post-POEM), healing of esophagitis is assessed.

Study Arms:

  • Arm A: Vonaprazan 20 mg once daily for 8 weeks
  • Arm B: Esomeprazole 40 mg once daily for 8 weeks

Study Procedures:

Baseline Assessment (3 Months Post-POEM, Before Randomization)

  • Upper GI Endoscopy: Confirmation of LA grade B or higher reflux esophagitis.
  • GERD-Q Score assessment.
  • Randomization to Vonaprazan 20 mg or Esomeprazole 40 mg. Follow-Up (Week 4 - Interim Visit)
  • GERD-Q Score assessment.

End-of-Treatment (Week 8 - Final Visit, 5 Months Post-POEM)

  • Upper GI Endoscopy to assess healing of reflux esophagitis.
  • GERD-Q Score reassessment.
  • Final adverse event reporting.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥18 years
  • History of POEM for achalasia
  • Endoscopic confirmation of LA grade B, C, or D reflux esophagitis at 3 months post-POEM
  • GERD symptoms (heartburn, regurgitation) for ≥4 weeks
  • Willingness to provide informed consent and comply with study procedures

Exclusion criteria

  • History of prior anti-reflux surgery
  • Presence of Barrett's esophagus, esophageal stricture, or malignancy
  • Severe gastroparesis or esophageal motility disorder unrelated to achalasia
  • Pregnancy or breastfeeding
  • Severe hepatic or renal impairment (ALT/AST >3× ULN, eGFR <30 mL/min)
  • Regular use of NSAIDs, steroids, or anticoagulants affecting esophageal healing

Treatment and study plan

Vonoprazan

Drug

a potassium-competitive acid blocker (P-CAB), offers superior acid suppression and may provide enhanced healing in post-POEM reflux esophagitis.

Other names: per oral endoscopy myotomy

Esomeprazole 40mg

Drug

It is a proton pump inhibitor which reduces the excessive acid secretion in the stomach and it heals grade B esophagitis (>5mm ulcer between two mucosal folds in esophagus)

Other names: per oral endoscopy myotomy

Primary outcomes

  1. • Endoscopic healing of reflux esophagitis at 8 weeks (absence of LA grade B or higher esophagitis).

    Time frame: 8 weeks

    This can be find during endoscopy test

Secondary outcomes

  1. • Improvement in GERD-Q scores at 8 weeks

    Time frame: 8 weeks

    GERD questionnaire can be calculated based on heart burn , regurgitation symptom scores which is scaled like 1 is very low symptoms, 5 is worse symptoms (outcome)

Study contacts

Contact information is provided by the study sponsor or research team.

Rajesh Goud Mr Maragoni, M.Pharm

CONTACT

[email protected]

04023378888 ext. 312

Zaheer Nabi Dr Mohammed, MD DNB

CONTACT

[email protected]

04023378888 ext. 427

Sponsors and collaborators

Lead sponsor

Asian Institute of Gastroenterology, India

Other

Registry information

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
May 2, 2025
Registry last updated
Apr 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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