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RecruitingNCT07662603Updated Jun 23, 2026

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

An interventional study of inspiratory muscle trianing in Behcet Disease, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to participants aged 13 Years to 17 Years. Per ClinicalTrials.gov, last updated 2026-06-23.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started May 2026; still recruiting 5 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
13 Years to 17 Years
Sex
All
01

Study summary

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

Read the detailed description

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.

02

Conditions studied

  • Behcet Disease

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03

In context

Behcet Syndrome

136 studies on the registry are indexed under Behcet Syndrome; 43 are open to participants now.

This study's planned enrollment of 40 is below the median of 50 across 70 interventional studies indexed under Behcet Syndrome.

Browse Behcet Syndrome studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
13 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • adlescent patients
  • complain Behcet disease
  • after pulmonary endoarterectomy

Exclusion criteria

Exclusion Criteria:

  • chronci cardiac diseases
  • psychic disease
  • mental disease
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • Experimental
    group number 1

    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)

    Other: inspiratory muscle trianing

  • No intervention
    group number 2

    twenty Behcet disease patients with pulmonary endoarterectomy will act as wailisting group for 12 weeks

Interventions

  • Otherinspiratory muscle trianing

    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)

06

What researchers measure

Primary outcomes

  1. forced vital capacity

    it si a pulmaonry fucntion test

    Time frame: it will be measured after 12 weeks

Secondary outcomes

  1. forced expiratory volume

    it will be assessed in first second of expiration

    Time frame: It will be measured after 12 weeks

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

    it is a pulmoanry fucntion test

    Time frame: It will be measured after 12 weeks

  3. fatigue severity scale

    it will assess fatigue perception

    Time frame: It will be measured after 12 weeks

  4. child health questainanire parent form assessment of phsyical summary

    it is an assessment of quality of life

    Time frame: it will be measured after 12 weeks

  5. child health questainanire parent form assessment of mental summary

    it is an assessment of quality of life

    Time frame: It will be measured after 12 weeks

  6. Ruffier index

    it an indiactor for cariorespiratory fitness

    Time frame: It will be measured after 12 weeks

  7. maxinmal inspiration pressure

    it is an indicator for isnpiratory msucular stength

    Time frame: It will be measured after 12 weeks

  8. maxinmal expiration pressure

    it is an indicator for expiratory msucular stength

    Time frame: It will be measured after 12 weeks

  9. six minute walk test

    distance covered during this test will be assessed

    Time frame: It will be measured after 12 weeks

07

Study locations

1 of 1 sites recruiting
  • Cairo University
    Giza, Dokki, Egypt
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07662603
Lead sponsor
Cairo University
Responsible party
Ali Mohamed Ali ismail (lecturer of physical therapy for Cardiovascular, Respiratory disorder and Geriatrics, Faculty of Physical Therapy, Cairo University, Cairo University) — Principal investigator
First posted
Jun 23, 2026
Start date
May 6, 2026
Primary completion
Sep 6, 2026 (estimated)
Completion
Sep 6, 2026 (estimated)
Last update
Jun 23, 2026

Study contacts

Ali MA Ismail, lecturer
Contact
ali.mohamed@pt.cu.edu.eg
01005154209
ali mohamed, lecturer
Contact
fatma1995@gmail.com
01031321109
Ali MA Ismail, lecturer
principal investigator · Cairo University

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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