Viewing Study NCT06551337



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06551337
Status: RECRUITING
Last Update Posted: None
First Post: 2024-08-05

Brief Title: Vitamin D Replacement in Bronchiectasis
Sponsor: None
Organization: None

Study Overview

Official Title: Prospective Clinical Study on Vitamin D Replacement in Bronchiectasis - A Pilot Study
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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 ie 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None