One Dose Versus Three Weekly Doses of Benzathine Penicillin G for Patients With Early Syphilis

Last updated: November 15, 2018
Sponsor: Jun Li
Overall Status: Active - Recruiting

Phase

4

Condition

Sexually Transmitted Diseases (Stds)

Rash

Gynecological Infections

Treatment

N/A

Clinical Study ID

NCT02857959
PUMCH-2016078
  • Ages 18-60
  • All Genders

Study Summary

The purpose of this study is to observe the serological response to 1 or 3 weekly doses of benzathine penicillin G in patients with early syphilis.

Eligibility Criteria

Inclusion

Inclusion Criteria:

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

  2. A rapid plasma reagin (RPR) test was positive, with a titer were 1:4 or higher. Inaddition, Treponema pallidum particle agglutination assay and/or fluorescenttreponemal antibody absorption test were reactive.

Exclusion

Exclusion Criteria:

1.Patients who were pregnancy, known allergy to penicillin, use of antibiotics activeagainst syphilis during the preceding six months for symptomatic cases or during thepreceding two years for asymptomatic cases, and concurrent illnesses requiring treatmentwith antibiotics effective against syphilis. 2. if RPR titers were found to be 1:4 or lessor the T. pallidum particle agglutination test was nonreactive, participants wereretrospectively excluded from the trial unless primary syphilis was confirmed by thefinding of T. pallidum in ulcer exudates on direct immunofluorescence

Study Design

Total Participants: 150
Study Start date:
August 01, 2016
Estimated Completion Date:
August 31, 2020

Connect with a study center

  • Department of Dermatology and Venereology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China

    Beijing,
    China

    Active - Recruiting

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