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Procedure
1 for Esophageal Achalasia
N/A
Waitlist Available
Led By David R Urbach, MD
Research Sponsored by University Health Network, Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up yrs 1 to 5
Awards & highlights
Study Summary
The purpose of this study is to compare pneumatic dilatation and laparoscopic Heller myotomy in patients with achalasia in order to learn which of these two treatments should be recommended to patients in the future.
Eligible Conditions
- Esophageal Achalasia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, m2, m6, yrs 1 to 5
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, m2, m6, yrs 1 to 5
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Esophageal Achalasia
Secondary outcome measures
Clinical outcomes of care including short term outcomes, major complications, and long-term clinical outcomes.
Gastroesophageal reflux as measured by ambulatory 24-hr esophageal pH measurement
Gastrointestinal disease-specific quality of life (GIQLI)
+2 moreTrial Design
2Treatment groups
Active Control
Group I: 1Active Control1 Intervention
pneumatic dilatation
Group II: 2Active Control1 Intervention
Laparoscopic myotomy
Find a Location
Who is running the clinical trial?
University Health Network, TorontoLead Sponsor
1,478 Previous Clinical Trials
485,344 Total Patients Enrolled
1 Trials studying Esophageal Achalasia
50 Patients Enrolled for Esophageal Achalasia
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,345 Previous Clinical Trials
26,453,458 Total Patients Enrolled
David R Urbach, MDPrincipal InvestigatorUniversity Health Network, Toronto
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