Achalasia Patient Reported Outcomes

Sponsor
Mayo Clinic (Other)
Overall Status
Recruiting
CT.gov ID
NCT02606578
Collaborator
(none)
100
1
84
1.2

Study Details

Study Description

Brief Summary

Patients that are either scheduled to undergo or have undergone an achalasia procedure at the Mayo Clinic Rochester are asked to participate. The purpose of this study is to gather information and determine if one of these procedures is superior to the other.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaires

Detailed Description

This is a non-randomized, non-inferiority trial that has been created to compare results of achalasia procedures including but not limited to: POEM + Partial Fundoplication (PF), POEM and Laparoscopic Modified Heller Myotomy + PF and POEM + Peroral Plication of the esophagus. Using a set of consistent evaluation tools for patients undergoing treatment for achalasia allows a standardized evaluation and comparison of these groups of patients. The long term and comparative POEM procedure outcomes are not currently known. Patients undergoing POEM, fundoplication, and/or laparoscopic myotomy report having varying degrees of symptoms of reflux, dysphagia, and pain. Providers also note varying degrees of esophagitis by endoscopy, reflux by impedance or pH scoring, and recurrence by repeat manometry. Many of these issues can be quantified using pH probe testing, upper GI endoscopy, high resolution manometry, CT scans, Endoflip device and esophagrams. There are various validated questionnaires that have been used to assess problem areas of reflux, dysphagia, and pain such as the Promis Global Health Score, Ekhardt Score, Mayo GER Score, Modified Dysphagia Questionnaire-30 Day, Zubrod Score, and pain scale. Each of these symptoms, tests, and questionnaires contributes to the provider's understanding of the patient's postoperative outcome.

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Achalasia Patient Reported Outcomes
Study Start Date :
Oct 1, 2015
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Oct 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Comparison of different surgical techniques with patient reported post-operative symptoms on the achalasia questionnaire [2 years]

    Comparison of surgical techniques evaluated from the patient's medical record using patient reported post-operative symptoms on the achalasia questionnaire. The achalasia questionnaire includes quality of life, pain, activity level, heart burn, acid regurgitation, reflux, dysphagia, and diet.

Eligibility Criteria

Criteria

Ages Eligible for Study:
19 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 18 years old

  • Undergoing a POEM or laparoscopic modified heller myotomy and anti-reflux procedures

  • Esophagus diameter less <8 cm on barium swallow test

Exclusion Criteria:
  • Pregnant

  • Diverticular disease of the esophagus

  • Barrett's esophagus

  • Extensive abdominal adhesions

  • <50% predicted FEV1 on pulmonary function testing

  • Cardiac ejection fraction <25%

  • Esophageal stricture from prior myotomy

  • Sigmoidization of the esophagus

  • More than one prior balloon dilation (>3 cm) or any prior dilation of 3 cm

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic Rochester Minnesota United States 55901

Sponsors and Collaborators

  • Mayo Clinic

Investigators

  • Principal Investigator: Shanda Blackmon, MD, MPH, FACS, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Shanda Blackmon, M.D., M.P.H., PI, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT02606578
Other Study ID Numbers:
  • 15-006921
First Posted:
Nov 17, 2015
Last Update Posted:
Sep 16, 2021
Last Verified:
Sep 1, 2021
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2021