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Clinical Trials/DRKS00004496
DRKS00004496
Completed
Not Applicable

Electromyographic diagnosis of the muscle function of the thigh in male adolescents with CF- a pilot study. - EMCF

Medizinische Hochschule Hannover0 sites26 target enrollmentSeptember 18, 2013
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ConditionsE84Cystic fibrosis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
E84
Sponsor
Medizinische Hochschule Hannover
Enrollment
26
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 18, 2013
End Date
February 1, 2013
Last Updated
last year
Study Type
Observational
Sex
Male

Investigators

Sponsor
Medizinische Hochschule Hannover

Eligibility Criteria

Inclusion Criteria

  • •CF\- Group:
  • •assured cystic fibrosis, existing consent form,
  • •patients must be able to carry out analyzable pulmonary function tests, a physical performance tests (Biodex) and a set of whole body vibration training
  • •stable clinical condition without acute respiratory disease in the last 4 weeks respectively without acute exacerbation of the basic disease
  • •no new additionally diagnosted diseases in the last 3 months
  • •Control group:
  • •existing consent form, patients must be able to carry out analyzable pulmonary function tests, a physical performance tests (Biodex) and a set of whole body vibration training

Exclusion Criteria

  • •Cf\- Group:
  • •patients with problematic microbes (cepacia, MRSA, multiresistant bacteria requiring an isolation)
  • •patients coming to an evaluation regarding a lung transplantation
  • •patients after lung transplantation
  • •patients with an acute respiratory disease in the last 4 weeks respectively with an acute exacerbation of the basic disease
  • •patients with an acute health risk resulting in a raised risk for unwanted side effects or influencing the quality of the study results patients with a good adjusted diabetes mellitus can participate
  • •Control group:
  • •existence of a serious cardiovascular disease, existence of a pulmonary disease, existing of a cardiac pacemaker or a defibrillator, patients with an acute health risk resulting in a raised risk for unwanted side effects or influencing the quality of the study results

Outcomes

Primary Outcomes

Not specified

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