Skip to main content
Clinical Trials/EUCTR2012-002792-34-GB
EUCTR2012-002792-34-GB
Active, not recruiting
Phase 1

Phenotyping bronchiectasis based on aetiology, exacerbation characteristics and response to erythromycin. - Phenotyping bronchiectasis over 2 years including a macrolide trial

niversity Hospitals Leicester NHS Trust0 sites90 target enrollmentMarch 13, 2014

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Bronchiectasis
Sponsor
niversity Hospitals Leicester NHS Trust
Enrollment
90
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 13, 2014
End Date
TBD
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
niversity Hospitals Leicester NHS Trust

Eligibility Criteria

Inclusion Criteria

  • Group 1 \- 40 participants over 2 years including the intervention
  • \- Patients who have clinical symptoms suggestive of bronchiectasis confirmed by CT scan.
  • \- Aged 18\-100\.
  • \- Ability to give valid consent.
  • \- Willingness to attend the hospital every 3 months for 2 years.
  • Group 2 \- 50 participants for baseline visit only
  • \- Patients who have clinical symptoms suggestive of bronchiectasis confirmed by CT scan.
  • \- Aged 18\-100\.
  • \- Ability to give valid consent.
  • \- Willingness to attend the hospital for a one off visit.

Exclusion Criteria

  • Group 1 \- 40 participants over 2 years including the intervention
  • \- Active TB.
  • \- Patients under 18 and over 100\.
  • \- Patients who are too unwell to attend visits.
  • \- Patients with known cystic fibrosis.
  • \- Patients with traction bronchiectasis secondary to fibrosis.
  • \- Patients who are unable to consent.
  • \- Patients already on long term antibiotics.
  • \- Patients with macrolide allergy / severe intolerance / prolonged QT interval.
  • \- Patients taking medication with a known interaction with erythromycin where the use is contraindicated, with the exception of simvastatin.

Outcomes

Primary Outcomes

Not specified

Similar Trials