Skip to main content
Clinical Trials/NCT01202929
NCT01202929
Withdrawn
Not Applicable

Correlation of High Resolution Esophageal Manometry With Symptoms

University of Louisville1 site in 1 countryFebruary 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Achalasia
Sponsor
University of Louisville
Locations
1
Primary Endpoint
Differences and similarities in patients with achalasia
Status
Withdrawn
Last Updated
9 years ago

Overview

Brief Summary

High Resolution Manometry is a new technology that utilizes 36 solid state sensors on a thin catheter spaced at 1-cm intervals. One can more effectively measure the pressure of the esophagus. It includes a sophisticated software to display the pressures data as color topography plot using time, length of the esophagus and pressure within the entire esophagus. It is unclear if this technology improvement actually correlates with patient's symptoms.

Detailed Description

In a 2007 retrospective study performed using this technology, 400 subjects referred to the motility lab underwent high resolution manometry (HRM) for complaints of dysphasia, gastroesophageal reflux disease, chest pain and miscellaneous complaints. HRM offered greater detail of individual contracting segments of the esophagus, including the duration of contraction and propagation of individual contractions. For example, a new subclass of achalasia was defined by HRM. In this classification, achalasia is divided into types 1, 2 and 3. Type 1 corresponds to classic achalasia (complete esophageal motor failure), type 2 is a compression achalasia (simultaneous panesophageal pressurization with aperistalsis), and type 3 is spastic achalasia with aperistalsis (100% spasm). However, it is unclear if this categorization represents a spectrum of disease among patients with achalasia, or it represents distinct subgroups of patients with different symptom presentation and etiology. This study will attempt to correlate the data from HRM to patient's chief compliants, symptom severity, and clinical presentation.

Registry
clinicaltrials.gov
Start Date
February 2010
End Date
August 2011
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Subjects who are referred to the motility lab to undergoing esophageal HRM for various clinical indications.

Exclusion Criteria

  • Pregnancy
  • Unable to give consent
  • Less than 18 years old

Outcomes

Primary Outcomes

Differences and similarities in patients with achalasia

Time Frame: at 24 months

To determine the differences and similarities in the clinical presentation of patients with type 1, 2 and 3 achalasia based on the Chicago classification for HRM

Secondary Outcomes

  • Esophageal dysmotility in patients with postfundoplication compliants(at 24 months)
  • HRM parameters(at 24 months)
  • Correlation between HRM and symptoms(At 24 months)
  • Esophageal dysmotility in patients with dysphagia and GERD symptoms(at 24 months)

Study Sites (1)

Loading locations...

Similar Trials