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NCT Number: NCT07662603

Behcet Disease Patients With Pulmonary Endoarterectomy: Outcomes of Program of Inspiratory Msucle Trianing

physical complications are common in Behcet disease patients with pulmonary endoarterectomy, so outcomes of program of inspiratory msucle trianing must be investigated

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Key information

Conditions

Behcet Disease Behcet Syndrome Cardiovascular Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities Eye Diseases Genetic Diseases, Inborn Hereditary Autoinflammatory Diseases Mouth Diseases Panuveitis Skin Diseases Skin Diseases, Genetic Skin Diseases, Vascular Skin and Connective Tissue Diseases Stomatognathic Diseases Uveal Diseases Uveitis Uveitis, Anterior Vascular Diseases Vasculitis

Age range

13 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Forty Behcet disease patients with pulmonary endoarterectomy will be assigned to group I or Group II. the patients will be adolescents, 20 patients in the group. Group I will recive program of inspiratory msucle trianing for 12 weeks (one session daily, except the last two days of the week) Group II will act waitlist group.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • adlescent patients
  • complain Behcet disease
  • after pulmonary endoarterectomy

Exclusion criteria

  • chronci cardiac diseases
  • psychic disease
  • mental disease

Treatment and study plan

inspiratory muscle trianing

Other

twenty Behcet disease patients with pulmonary endoarterectomy will be will recive program of inspiratory msucle trianing for 12 weeks (one session daily, except the last two days of the week)

Primary outcomes

  1. forced vital capacity

    Time frame: it will be measured after 12 weeks

    it si a pulmaonry fucntion test

Secondary outcomes

  1. forced expiratory volume

    Time frame: It will be measured after 12 weeks

    it will be assessed in first second of expiration

  2. ratio of force vital capcity to first-second-expiratory forced expiration volume

    Time frame: It will be measured after 12 weeks

    it is a pulmoanry fucntion test

  3. fatigue severity scale

    Time frame: It will be measured after 12 weeks

    it will assess fatigue perception

  4. child health questainanire parent form assessment of phsyical summary

    Time frame: it will be measured after 12 weeks

    it is an assessment of quality of life

  5. child health questainanire parent form assessment of mental summary

    Time frame: It will be measured after 12 weeks

    it is an assessment of quality of life

  6. Ruffier index

    Time frame: It will be measured after 12 weeks

    it an indiactor for cariorespiratory fitness

  7. maxinmal inspiration pressure

    Time frame: It will be measured after 12 weeks

    it is an indicator for isnpiratory msucular stength

  8. maxinmal expiration pressure

    Time frame: It will be measured after 12 weeks

    it is an indicator for expiratory msucular stength

  9. six minute walk test

    Time frame: It will be measured after 12 weeks

    distance covered during this test will be assessed

Study contacts

Contact information is provided by the study sponsor or research team.

Ali MA Ismail, lecturer

CONTACT

[email protected]

01005154209

ali mohamed, lecturer

CONTACT

[email protected]

01031321109

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Jun 23, 2026
Registry last updated
Jun 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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