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Study of Bronchiectasis and Associated Cardiovascular Comorbidities

A

Assiut University

Status

Enrolling

Conditions

Bronchiectasis

Treatments

Device: Echocardiography

Study type

Observational

Funder types

Other

Identifiers

NCT05783869
23455668

Details and patient eligibility

About

Effect of cardiovascular comorbidities on disease severity and quality of life in Patients with acute exacerbation of non-cystic fibrosis bronchiectasis

Full description

The study will include patients with bronchiectasis, and in an attempt to correlate the effect and burden of cardiovascular comorbidities in those patients, we will study the quality of life in those patients in comparison to the control group ( patients with bronchiectasis and without any other comorbidities) using SF-36 quality of life questionnaire. We will also study the inflammatory markers in both groups using D-dimer, BNP, and CRP and correlate them with the frequency of hospital admission, the severity of symptoms, and the general health state.

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

• Any Patients with Bronchiectasis had no comorbidities other than cardiovascular comorbidities during the study period.

Exclusion criteria

  • Any Patients who refuse to participate in the study.
  • Any other comorbidity or end-organ failure may affect the study's result.

Trial design

30 participants in 2 patient groups

Patient with bronchiectasis and cardiovascular comorbidities
Description:
Patients with Bronchiectasis had no comorbidities other than cardiovascular comorbidities during the study period.
Treatment:
Device: Echocardiography
Patients with bronchiectasis and without cardiovascular comorbidities
Description:
Patients with Bronchiectasis had no comorbidities.
Treatment:
Device: Echocardiography

Trial contacts and locations

1

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Central trial contact

Ahmad Shaddad, MD; Shaadad Shaddad, MD

Data sourced from clinicaltrials.gov

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