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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03151902
Other study ID # HaEmekMC1
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 2, 2017
Est. completion date September 30, 2023

Study information

Verified date March 2022
Source HaEmek Medical Center, Israel
Contact Menachem Rottem, MD
Phone +972-528617823
Email rottem_me@clalit.org.il
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Blood samples from urticaria patients will be analyzed for viral particles


Description:

After digestion with DNase to eliminate human DNA, RNA will be reversed-transcribed and amplified with random primer/ Amplification products will be pooled and sequenced/ After substruction of sequences of vertebrates and highly repetitive sequences, contiguous sequences will be assembled and compared with motifs represented in databases of viruses. which will enable identification of putative protein sequences consistent with viruses


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date September 30, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients with chronic spontaneous urticaria Exclusion Criteria: - none

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Emek Medical Center Afula

Sponsors (1)

Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary viral particles presence of viral particels 6 months
See also
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