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NCT02871505 Clinical Trial

The Association Between Molecular Typing of Treponema Pallidum and Treatment Efficacy and Clinical Findings

Syphilis Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT02871505
Other study ID # PUMCH-2016079
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date August 2016
Est. completion date August 2020

Study information
Verified date November 2018
Source Peking Union Medical College Hospital
Contact Jun Li, M.D.
Phone 86-010-69151504
Email lijun35@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The investigators compare the treatment results and clicical presentations of different Molecular subtyping of Treponema pallidum

Recruitment information / eligibility
Status Recruiting
Enrollment 150
Est. completion date August 2020
Est. primary completion date August 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria

1. Persons with confirmed early symptomatic syphilis (primary or secondary) or high-titer latent syphilis

Exclusion Criteria:

1. Pregnant woman

2. Known allergy to penicillin

3. RPR titers were found to be 1:8 or less

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Benzathine Penicillin G

Locations
Country Name City State
China Department of Dermatology and Venereology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China Beijing

Sponsors (1)
Lead Sponsor Collaborator
Peking Union Medical College Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary rapid plasma regain titer 6 months after treatment
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