Vitamin D Replacement in Bronchiectasis
Recruiting now · Phase 4
Conditions studied: Bronchiectasis
In brief
This study seeks to address the limitations in previous related studies on vitamin D replacement and bronchiectasis exacerbation occurrence through a self-controlled pilot study. The investigators aim to investigate whether vitamin D replacement in bronchiectasis patients with vitamin D deficiency can reduce hospitalized bronchiectasis exacerbation occurrence. Patients who participated in the prior study entitled "Prospective clinical study on serum 25-hydroxyvitamin D (25-OH D) level and risk of bronchiectasis exacerbation" (UW 22-317) will be invited for participation during regular clinic follow-up and management in Queen Mary Hospital. If participants are willing to join the further research, participants will be recruited in this self-controlled study. There are some differences from usual management to non-CF bronchiectasis subjects. The study subjects would be checked for their blood 25-hydroxyvitamin-D level during the study period. The non-CF bronchiectasis subjects with Vitamin D deficiency would be given 1000 IU and 2000 IU (if needed). The investigators aim to correct their Vitamin D deficiency completely, aiming at blood 25-hydroxyvitamin-D level \>=50, i.e. treat to target. The dose depends on the level of Vitamin D after replacement. If blood 25-hydroxyvitamin-D level is 50 or above, then 1000 IU is suffice. If blood 25-hydroxyvitamin-D level is still below 50, the investigators will increase to 2000 IU.
Key facts
- Study ID
- NCT06551337
- Run by
- Queen Mary Hospital, Hong Kong
- People needed
- 104
- Starts
- 2024-04-17
- Expected to finish
- 2027-06-30
- Last updated by the study team
- 2024-08-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- ages 18 years or above, male or female.
- confirmed diagnosis of non-CF bronchiectasis based on high-resolution computed tomography (HRCT) scan.
- participation in the prior study entitled "Prospective clinical study on serum 25-hydroxyvitamin D (25-OH D) level and risk of bronchiectasis exacerbation" (UW 22-317)
You may not qualify if…
- underlying asthma, COPD and other co-existing respiratory diseases
- underlying osteoporosis
- supplementary Vitamin D in their regimen
- advanced chronic kidney disease with estimated glomerular filtration rate (eGFR) < 30mL/min
Where it is running
- Queen Mary Hospital — Hong Kong, Hong Kong (enrolling)
Full record on ClinicalTrials.gov
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