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PREcision MEDicine In Achalasia (PREMEDIA) - Cohort

RecruitingObservational study

PREcision MEDicine In Achalasia - A Multicenter Randomized Non-Inferiority Clinical Trial of Short Tailored POEM vs. Standard POEM for Non-Spastic Achalasia and A Multicenter Prospective Cohort Study of Long Tailored POEM for Spastic Esophageal Motility Disorders

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

1. Age ≥ 18
2. Type III achalasia or EGJOO with spastic/hypercontractile features or Jackhammer Esophagus or Distal Esophageal Spasm
3. Eckardt Score \> 3

Exclusion Criteria:

* Exclusion:

  1. Prior POEM
  2. Prior surgical treatment for achalasia
  3. Endoscopic pneumatic dilation or lower esophageal sphincter botulinum toxin (botox) injection within 6 months
  4. Prior unrelated esophageal or upper gastric surgery, including Roux-en-Y gastric bypass and sleeve gastrectomy
  5. Prior endoscopic gastroesophageal intervention for obesity or GERD, such endoscopic sleeve gastroplasty or transoral incisionless fundoplication
  6. Known secondary achalasia related to malignancy (pseudoachalasia)
  7. Known eosinophilic esophagitis
  8. Diverticulum (\> 2 cm) in distal esophagus
  9. Megaesophagus
  10. Fibroinflammatory stricture of the esophagus due to any etiology (e.g., peptic, radiation, eosinophilic)
  11. Pregnancy
  12. Standard contraindications to general anesthesia
  13. Standard contraindications to endoscopic myotomy in the esophagus (e.g. untreated varices)
  14. Unwillingness or inability to consent for the study
  15. Anticipated inability to follow protocol

About the study

The goal of this observational study is to learn about how the doctor decides how long to cut t the esophageal muscle during Per-Oral Endoscopic Myotomy (POEM) in patients with difficulty swallowing due to certain conditions. The main question it aims to answer is: does pre-POEM testing help the physician choose how long to cut the muscle.

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.

Sponsor: Northwestern University · Participants: 200 · Started: Dec 1, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07293689

Locations in the U.S.

ArizonaMayo Clinic Arizona, Scottsdale (Not yet recruiting)
CaliforniaUniversity of California San Diego, La Jolla (Not yet recruiting)
ColoradoUniversity of Colorado Denver, Denver (Not yet recruiting)
FloridaUniversity of Florida, Gainesville
Adventist Health System/Sunbelt, Inc, Orlando (Not yet recruiting)
GeorgiaEmory University, Atlanta
IllinoisNorthwestern University, Chicago
MarylandJohns Hopkins University, Baltimore (Not yet recruiting)
MassachusettsMassachusetts General Hospital, Boston
MissouriWashington University, St Louis (Not yet recruiting)
New YorkWeill Cornell Medical College, New York (Not yet recruiting)
North CarolinaAtrium Health/Wake Forest, Charlotte
OhioCase Western Reserve University, Cleveland (Not yet recruiting)
MetroHealth Medical Center, Cleveland
TennesseeVanderbilt University Medical Center, Nashville
TexasBaylor Scott & White Health, Dallas (Not yet recruiting)

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.