PREcision MEDicine In Achalasia (PREMEDIA)

Part of paid clinical trials in Scottsdale, Arizona.

Sponsor
Northwestern University
Study ID
NCT07293650
Phase
PHASE3
Status
Recruiting

Conditions

  • EGJ Outflow Obstruction Without Spastic/Hypercontractile Features
  • Type I Achalasia
  • Type II Achalasia

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Standard Myotomy — PROCEDURE
    Myotomy during POEM of 8-10 cm in length, extending 2-3 cm into the gastric cardia; intention to perform selective circular myotomy, but allowing full thickness myotomy. FLIP is used to confirm adequate myotomy.
  • Tailored Short Myotomy — PROCEDURE
    Myotomy during POEM of 4-5 cm in length, extending 1-2 cm into the gastric cardia; intend to perform selective circular myotomy, but allowing full thickness myotomy. FLIP is used to confirm adequate myotomy.

Study Details

The goal of this clinical trial is to learn if shorter Per-Oral Endoscopic Myotomy (POEM) works as well as a longer POEM in patients with trouble swallowing due to certain conditions. The main question\[s\] it aims to answer \[is/are\]: * Does making a smaller cut in the muscle at the bottom of the esophagus work just as well as making the standard bigger cut in relieving symptoms? * Does making the smaller cut reduce the side effects of the procedure compared to the standard bigger cut? Researchers will compare the symptoms and side effects of making a shorter cut to the symptoms and side effects of a longer cut. Participants will allow researchers to access their standard of care information in their medical record, complete questionnaires at up to 6 times over a 2-year period.

Key Dates

Start date
Apr 23, 2026
Status verified
Apr 2026
Primary completion
Apr 1, 2029
Completion
Mar 1, 2030

Study Design

Enrollment
372 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Standard Myotomy
  • Experimental: Tailored Short Myotomy

Primary Outcome Measure

Clinical Response-Overall [ Time Frame: From enrollment to Year 2 ]

Central Contacts

Locations (13)

FacilityCityStateZIPSite coordinators
Mayo Clinic ArizonaScottsdaleArizona85259-
University of California San DiegoLa JollaCalifornia92093-
University of Colorado DenverDenverColorado80217-
University of FloridaGainesvilleFlorida32611-
Adventist Health System/Sunbelt, IncOrlandoFlorida32803-
Emory UniversityAtlantaGeorgia30322-
Northwestern UniversityChicagoIllinois60611
312-926-4525
John Pandolfino, MD (PRINCIPAL_INVESTIGATOR)
Johns Hopkins UniversityBaltimoreMaryland21218-
Washington UniversitySt LouisMissouri63130-
Weill Cornell Medical CollegeNew YorkNew York10065-
Case Western Reserve UniversityClevelandOhio44106-
Vanderbilt University Medical CenterNashvilleTennessee37232-
Baylor Scott & White HealthDallasTexas75204-

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