3 Year Follow up on ANO5 Patients

Sponsor
Rigshospitalet, Denmark (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05206617
Collaborator
(none)
17
1
61.9
0.3

Study Details

Study Description

Brief Summary

The aim of the study is to investigate progression in muscle affection in patients with pathogenic variants in the anoctamin 5 gene to:

  1. investigate possible progression of disease over time

  2. investigate good and reliable outcome measures

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention - pure observational study

Detailed Description

Muscles of patients with pathogenic variants in the anoctamin 5 gene will over time be infiltrated with fat. This is especially visible on MRI and can be seen even before any symptoms appear. MRI is thus used increasingly to investigate muscle affection in neuromuscular disorders. Together with functional measurements it is possible to describe how patients are affected clinically and subclinically. There are still many things that need covering - rate of progression is undertermined and good outcome measures are still needed for future clinical trials.

Muscles of the whole body in patients with neuromuscular disorders will be investigated 3 times through a 3 year follow-up study.

The aim of the study is to investigate progression in muscle affection in patients with pathogenic variants in the anoctamin 5 gene to:

  1. investigate possible progression of disease over time

  2. investigate good and reliable outcome measures

Study Design

Study Type:
Observational
Actual Enrollment :
17 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
3 Year Follow up on Patients With Pathogenic Anoctamin 5 Variants
Actual Study Start Date :
Jan 1, 2018
Anticipated Primary Completion Date :
Mar 1, 2022
Anticipated Study Completion Date :
Mar 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Limb Girdle Muscular Dystrophy type 2L

At baseline, 1- and 3-year follow up will the outcome measures be assessed. There will be no intervention.

Other: No intervention - pure observational study
No intervention

Outcome Measures

Primary Outcome Measures

  1. Change in fat fraction during 3 years [40 minutes]

    Change in fat fraction (%) during 3 years in muscles from the whole body measured from Dixon MRI.

Secondary Outcome Measures

  1. Change in fatigue during 3 years [5 minutes]

    Change in fatigue during 3 years measured through the questionnaire 'fatigue severity score', FSS. 9 questions scoring from 1-7 where 7 correlates to "strongly agree". Higher score means more fatigue.

  2. Change in quality of life during 3 years [15 minutes]

    Change in quality of life during 3 years measured through the questionnaire SF36. 36 questions. Higher score means higher quality of life.

  3. Change in pain and function during 3 years [10 minutes]

    Change in pain and function in lower limbs during 3 years measured through the questionnaire 'low back pain rating scale ', LBPRS. 6 questions rated from 0-10 with 0 meaning no pain. Higher score means more pain.

  4. Change in motor function during 3 years [30 minutes]

    Change in motor function during 3 years measured using the test the Motor Function Measure 32. 32 tasks to do, each task score 0-3. Higher score means better motor function.

  5. Change in handgrip during 3 years [10 minutes]

    Change in handgrip during 3 years measured using a handgrip dynamometer.

  6. Change in whole body muscle strenght during 3 years [30 minutes]

    Change in muscle strenght in whole body during 3 years measured using the technique 'manual muscle testning (MMT)' and the 'manual rating scale (MRC) '

  7. Change in muscle strenght during 3 years [30 minutes]

    Change in muscle strenght in knee, hip and back during 3 years measured using a staionary dynamometer (a biodex dynamometer)

  8. Change in balance during 3 years [20 minutes]

    Change in balance during 3 years measured using a biosway

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Pathogenic variant in the anoctamin 5 gene

  • Age more than 18 years

Exclusion Criteria:

None

Contacts and Locations

Locations

Site City State Country Postal Code
1 Copenhagen Neuromuscular Center Copenhagen Region Hovedstaden Denmark 2100

Sponsors and Collaborators

  • Rigshospitalet, Denmark

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nanna Scharff Poulsen, Principal investigator, Rigshospitalet, Denmark
ClinicalTrials.gov Identifier:
NCT05206617
Other Study ID Numbers:
  • H-16030358
First Posted:
Jan 25, 2022
Last Update Posted:
Feb 4, 2022
Last Verified:
Jan 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nanna Scharff Poulsen, Principal investigator, Rigshospitalet, Denmark
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 4, 2022