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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 9 October 2023
Main ID:  NCT01908543
Date of registration: 23/07/2013
Prospective Registration: No
Primary sponsor: Imperial College London
Public title: Iron Deficiency and Hereditary Haemorrhagic Telangiectasia
Scientific title: Iron Deficiency and Hereditary Haemorrhagic Telangiectasia
Date of first enrolment: July 2013
Target sample size: 3
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/ct2/show/NCT01908543
Study type:  Interventional
Study design:  Allocation: N/A. Intervention model: Single Group Assignment. Primary purpose: Treatment. Masking: None (Open Label).  
Phase:  N/A
Countries of recruitment
United Kingdom
Contacts
Name:     Claire L Shovlin, PhD FRCP
Address: 
Telephone:
Email:
Affiliation:  Imperial College London
Key inclusion & exclusion criteria

Inclusion Criteria:

- Hereditary haemorrhagic telangiectasia (HHT). Definite diagnosis of HHT by
international criteria.

- No iron tablets or treatment taken on day of assessment

- Ability to provide informed consent.

Exclusion Criteria:

- Inability to provide informed consent

- Intercurrent infection or illness predicted to modify iron absorption.

- Needle phobia.



Age minimum: 18 Years
Age maximum: 80 Years
Gender: All
Health Condition(s) or Problem(s) studied
Hereditary Haemorrhagic Telangiectasia
Intervention(s)
Drug: Ferrous sulphate 200mg oral tablet
Primary Outcome(s)
Blood iron indices [Time Frame: 4-5 hours after iron tablet ingestion]
Secondary Outcome(s)
Secondary ID(s)
CLS 2013/1
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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