Hereditary Haemorrhagic Telangiectasia (HHT) Clinical Trial
Official title:
Immunmodulation in Patients With HHT
NCT number | NCT02983253 |
Other study ID # | ImmunUHEssen |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | June 2016 |
Est. completion date | October 2019 |
Verified date | December 2019 |
Source | University Hospital, Essen |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Hereditary haemorrhagic telangiectasia (HHT), also known as Rendu-Osler-Weber syndrome, is an
inherited multisystemic disorder. Literature suggests that HHT is often associated with
higher frequency of infectious diseases.
The purpose of this study is to evaluate a variety of immunologic parameters in the blood
serum of HHT patients in comparison to probands.
Status | Completed |
Enrollment | 124 |
Est. completion date | October 2019 |
Est. primary completion date | October 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - aged 18 or over, HHT Exclusion Criteria: - Unable to provide informed consent |
Country | Name | City | State |
---|---|---|---|
Germany | University Hospital Essen | Essen |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Essen |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Functional properties of leucocytes in patients with HHT | November 2016 - December 2018 | ||
Other | Differences in size of leucocytes in patients with HHT | November 2016 - December 2018 | ||
Primary | Amounts of leucocytes in patients with HHT | November 2016 - December 2018 | ||
Secondary | Differences in distribution of leucocytes in patients with HHT | November 2016 - December 2018 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
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