Identification of Tongue Involvement in Late-Onset Pompe Disease

Sponsor
Duke University (Other)
Overall Status
Completed
CT.gov ID
NCT02765828
Collaborator
Genzyme, a Sanofi Company (Industry)
73
1
37.7
1.9

Study Details

Study Description

Brief Summary

This purpose of this study is to determine if tongue strength and tongue ultrasound measurements differentiates patients with untreated late-onset Pompe Disease (LOPD) from patients with acquires/hereditary myopathies or neuropathies. It is hypothesized that abnormalities in tongue function and structure in patients with LOPD may be useful in discriminating this condition from others that have similar presentations.

Condition or Disease Intervention/Treatment Phase
  • Other: Observational study

Study Design

Study Type:
Observational
Actual Enrollment :
73 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Determining the Diagnostic Utility of the Identification of Tongue Involvement in Late-Onset Pompe Disease (LOPD)
Actual Study Start Date :
May 25, 2016
Actual Primary Completion Date :
Jul 15, 2019
Actual Study Completion Date :
Jul 15, 2019

Arms and Interventions

Arm Intervention/Treatment
Late-Onset Pompe Disease

Other: Observational study
The following exams will be done in all cohorts: tongue manual muscle testing (MMT), tongue quantitative muscle testing, tongue ultrasound measurements

Acquired/Hereditary Myopathy

Other: Observational study
The following exams will be done in all cohorts: tongue manual muscle testing (MMT), tongue quantitative muscle testing, tongue ultrasound measurements

Neuropathy

Other: Observational study
The following exams will be done in all cohorts: tongue manual muscle testing (MMT), tongue quantitative muscle testing, tongue ultrasound measurements

Outcome Measures

Primary Outcome Measures

  1. Maximal lingual (tongue) strength measured via manual muscle testing (MMT) measured via ordinal scale (see description) [Day 1]

    Lingual strength will be rated with a validated 0-4 ordinal scale. Score Description 0 - Normal strength, no weakness. - Mild weakness. The tongue can be overcome with effort. - Moderate weakness. Easy to overcome. - Minimal movement. Unable to protrude to either side. - No movement detected.

  2. Maximal lingual (tongue) strength measured via quantitative muscle testing (QMT) measured in kilopascals (KPA) [Day 1]

Secondary Outcome Measures

  1. Maximal muscle thickness measured with ultrasound assessment in millimeters (mm) [Day 1]

    Comprises part of assessment of lingual (tongue) structure via qualitative tongue ultrasound assessment. On-screen calipers will be used to perform measurement.

  2. Echo intensity measured with ultrasound assessment utilizing grayscale analysis [Day 1]

    Comprises part of assessment of lingual (tongue) structure via qualitative tongue ultrasound assessment. Echo intensity measurements consist of drawing a box over subcutaneous tissue and muscle areas of interest using the grayscale histogram function. This number will be recorded along with the standard deviation (grayscale analysis).

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age ≥ 12 years

  • confirmed diagnosis of LOPD and naïve to enzyme-replacement therapy (ERT)

  • acquired/hereditary myopathy (e.g., dermatomyositis, polymyositis, inclusion body myositis, limb-girdle muscular dystrophy, distal myopathy, myotonic muscular dystrophy, and other myopathy)

  • neuropathy (e.g., peripheral neuropathy, cranial neuropathy, autonomic neuropathy, focal neuropathy)

Exclusion Criteria:
  • current use, history within the past two years of use, or eligible but declined use of Lumizyme® enzyme replacement therapy (applicable to LOPD group)

  • history of stroke, Parkinson's disease, oculopharyngeal muscular dystrophy, head and neck cancer or radiation treatment to head/neck, or other conditions that commonly affect lingual strength

  • inability to follow directions for study participation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Duke University Medical Center Durham North Carolina United States 27710

Sponsors and Collaborators

  • Duke University
  • Genzyme, a Sanofi Company

Investigators

  • Principal Investigator: Harrison Jones, PhD, Division of Head and Neck Surgery & Communication Sciences, Duke University Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Duke University
ClinicalTrials.gov Identifier:
NCT02765828
Other Study ID Numbers:
  • Pro00068729
First Posted:
May 9, 2016
Last Update Posted:
Jul 6, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 6, 2021