Cystic Fibrosis Trial, Recruiting NCT07599839 Sponsor: Assiut University Condition: Cystic Fibrosis
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Cystic Fibrosis Trial, Recruiting

NCT07599839
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 years or older
  • People who have been diagnosed with non-cystic fibrosis bronchiectasis (a lung condition causing widened, damaged airways — but not caused by cystic fibrosis), confirmed by a clinical assessment and a detailed CT scan of the chest
  • People whose condition is currently stable or being monitored as part of routine care, and who are being assessed for how severe their condition is
  • People who are attending outpatient clinics, hospital wards, or respiratory follow-up services at Assiut University Hospitals during the time the study is enrolling participants
  • People who are able to take part in a structured assessment of their bronchiectasis severity using a specific framework called the BASE framework
  • People who are able to complete the routine clinical tests required by the study, including breathing tests, imaging, oxygen level checks, and blood tests
  • People who are able to attend follow-up appointments over 12 months to track their condition and any flare-ups
  • People who have given written consent to take part, or whose legal representative has done so on their behalf

Who may not be able to join:

  • People whose bronchiectasis is caused by cystic fibrosis
  • People whose main lung diagnosis is advanced scarring lung disease that has caused the airways to widen as a side effect (confirm with trial site)
  • People who have active tuberculosis (TB) of the lungs at the time of enrolment
  • People who have an active lung infection caused by a type of bacteria called nontuberculous mycobacteria, which is currently being treated
  • People who have an active cancer or a serious non-lung illness that is expected to prevent them from completing 12 months of follow-up
  • People who have a severe, life-threatening illness at the time of enrolment that would make it unsafe to participate
  • People who have recently had major chest surgery or a serious chest injury that would interfere with the initial assessments
  • People who are unable to complete the required tests and assessments at the start of the study
  • People who are unable or unwilling to attend follow-up appointments over the 12-month period
  • People who do not wish to participate

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Ahmad M Shaddad, MD, Assiut University

Phone: +201111171930

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
11 September 2025
Est. completion
1 January 2027

Where this trial is recruiting

🇪🇬 Egypt

Primary endpoints

Twelve-Month Bronchiectasis Exacerbation Risk Predicted by the BASE Prognostic Model (BASE-P)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov