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Diet and Hereditary Haemorrhagic Telangiectasia

NCT01692015 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-03-29

Study results available
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Summary

Hereditary Haemorrhagic Telangiectasia (HHT) affects 1 in 5,000 people. The purpose of this study is to provide data regarding the diet and nosebleed frequency using a questionnaire.

This will be filled in by people with HHT.

The questionnaire has been designed in paper format.

Conditions

  • Hereditary Haemorrhagic Telangiectasia (HHT)

Interventions

OTHER

Questionnaire on dietary history

OTHER

Questionnaire on nosebleed severity

OTHER

One week food diary generated by weighing foods

PROCEDURE

Blood tests for full blood count, albumin, and indices of nutritional status

Sponsors & Collaborators

  • Imperial College London

    lead OTHER

Principal Investigators

  • Claire L Shovlin, PhD FRCP · Imperial College London

Study Design

Allocation
NON_RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2013-09-30
Completion
2016-09-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01692015 on ClinicalTrials.gov