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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT03310424
Other study ID # 14423
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 27, 2017
Est. completion date August 2024

Study information

Verified date October 2023
Source London School of Hygiene and Tropical Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Syphilis is an important sexually transmitted infection. There has been an epidemic of syphilis amongst men who have sex with men in the United Kingdom in the last decade. Early infection with syphilis causes a genital ulcer followed, in the absence of treatment, by a generalised illness often accompanied by rash. Studies on the pathogenesis of syphilis have been limited because it is not possible to grow syphilis outside of the body. New approaches using molecular tests allow the immune response of the patient to infection to be measured directly from a swab of a genital ulcer or rash and/or a blood sample and also allow the whole genetic sequence of the bacteria to be obtained from a swab. In this study the investigators will collect swabs from ulcers or rashes and a blood sample from patients with syphilis and measure both the response of the patient immune system and the genetic sequence of the bacteria. Patients will be enrolled at sexual health clinics in the United Kingdom. Patients will receive standard medical care including standard treatment for syphilis in line with national guidelines. Standard management already includes collection of a swab and a blood sample. For this study an additional swab sample and an additional 5ml of blood will be collected for use in this research project. By better understanding host immune system responds to infection with syphilis the studies aims to gain better insights in to the pathogenesis of this important sexually transmitted disease.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 46
Est. completion date August 2024
Est. primary completion date July 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Early infectious syphilis with exudative skin/genital lesions from which a lesion swab can be obtained Exclusion Criteria: - Age <18 years - Unable to provide consent - Patients with other stages of syphilis apart from Primary or Secondary OR patients without a lesion from which swabs can be obtained

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No active intervention.
No active intervention is undertaken. Collection of samples for bio-informatic analysis only

Locations

Country Name City State
United Kingdom Mortimer Market Centre London

Sponsors (1)

Lead Sponsor Collaborator
London School of Hygiene and Tropical Medicine

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Whole Genome Sequencing Whole Genome Sequencing of T.pallidum From samples collected at baseline
Primary Host Transcriptomic Response RNA Sequencing from lesion and blood samples From samples collected at baseline
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