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Trial record 10 of 95 for:    Recruiting, Not yet recruiting, Available Studies | "Muscular Dystrophies"

Prognostic Factors Affecting Duchenne Muscular Dystrophy

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ClinicalTrials.gov Identifier: NCT03372655
Recruitment Status : Not yet recruiting
First Posted : December 14, 2017
Last Update Posted : December 14, 2017
Sponsor:
Information provided by (Responsible Party):
Nehal Refaat Mohammed, Assiut University

Brief Summary:
Determination of prognostic factors affecting ambulation of duchenne muscular dystrophy

Condition or disease
Duchenne Muscular Dystrophy

Detailed Description:
Duchenne muscular dystrophy is the most common herditary muscular disease , it lead to loss of ambulation in early teenageers . It lead to early death at the mean age of 19 years

Study Type : Observational
Estimated Enrollment : 82 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Prognstic Factors Affecting Duchenne Muscular Dystrophy
Estimated Study Start Date : January 1, 2018
Estimated Primary Completion Date : January 1, 2019
Estimated Study Completion Date : March 1, 2019





Primary Outcome Measures :
  1. Ten meter walking test [ Time Frame: 2018 - 2019 ]
    Questionnaire


Secondary Outcome Measures :
  1. Muscle strenght [ Time Frame: 2018- 2019 ]
    Questionnaire



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Ages Eligible for Study:   10 Years to 18 Years   (Child, Adult)
Sexes Eligible for Study:   Male
Gender Based Eligibility:   Yes
Sampling Method:   Non-Probability Sample
Study Population
Male patient diagnosed as duchenne muscular dystrophy by typical clinical picture&shooting serum CPK level & EMG study or biopsy
Criteria

Inclusion Criteria:

  • any male pt diagnosed as duchenne muscular dystrophy by typical clinical picture &shooting serum CPK level &EMG study or biopsy & age 10 to 18yrs old

Exclusion Criteria:

  • female patient ' age below 10 yrs old or above 18 yrs old .patient with autoimmune disease or malignancy

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03372655


Contacts
Contact: Nehal Refaat, Residant 01000242438 nehalrefaatmohammed@gmail.com

Sponsors and Collaborators
Assiut University

Responsible Party: Nehal Refaat Mohammed, Sponsor investigator, Assiut University
ClinicalTrials.gov Identifier: NCT03372655     History of Changes
Other Study ID Numbers: PFADMD
First Posted: December 14, 2017    Key Record Dates
Last Update Posted: December 14, 2017
Last Verified: December 2017

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No

Additional relevant MeSH terms:
Muscular Dystrophies
Muscular Dystrophy, Duchenne
Muscular Disorders, Atrophic
Muscular Diseases
Musculoskeletal Diseases
Neuromuscular Diseases
Nervous System Diseases
Genetic Diseases, Inborn
Genetic Diseases, X-Linked