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Treatment Responses of Early Syphilis to Ceftriaxone Plus Doxycycline

Primary Purpose

Early Syphilis

Status
Recruiting
Phase
Phase 4
Locations
Taiwan
Study Type
Interventional
Intervention
Doxycycline
Ceftriaxone
benzathine penicillin G
Sponsored by
National Taiwan University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Early Syphilis

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: PLWH aged 20 years or more PLWH with early syphilis (i.e. primary, secondary, or early latent syphilis), confirmed by a positive rapid plasma reagin (RPR) titer with a reactive Treponema pallidum particle agglutination (TPPA) assay. PLWH has provided informed consent Exclusion Criteria: PLWH with RPR titers of less than 4 Exposure to antibiotics with activity against T. pallidum, such as penicillins, third- generation cephems, doxycycline, or macrolides, within the preceding 4 weeks A known or suspected infection other than syphilis requiring additional treatment with an antimicrobial active against T. pallidum A history of intolerance to penicillin, ceftriaxone, or doxycycline Pregnancy

Sites / Locations

  • Kuan-Yin LinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

single-dose ceftriaxone plus doxycycline

single-dose BPG plus doxycycline

Arm Description

single-dose ceftriaxone (1g intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)

single-dose BPG (2.4 MU intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)

Outcomes

Primary Outcome Measures

Rate of serologic response at month 6
Serologic response is defined as either a 4-fold or greater decline in RPR titer compared to baseline or being RPR-nonreactive

Secondary Outcome Measures

Rate of microbiologic response of syphilis at week 4
Microbiologic response of syphilis is defined as T. pallidum PCR Ct value >38
Rate of microbiologic response of bacterial STIs at week 4
Microbiologic response of bacterial STIs is defined as negative PCR results
Rate of serologic response at months 3 and 12
Serologic response is defined as either a 4-fold or greater decline in RPR titer compared to baseline or being RPR-nonreactive

Full Information

First Posted
March 8, 2023
Last Updated
July 31, 2023
Sponsor
National Taiwan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05980871
Brief Title
Treatment Responses of Early Syphilis to Ceftriaxone Plus Doxycycline
Official Title
Treatment Responses of Early Syphilis to Single-dose Ceftriaxone Plus Doxycycline Versus Single-dose Benzathine Penicillin G Plus Doxycycline in PLWH
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 10, 2023 (Actual)
Primary Completion Date
March 15, 2025 (Anticipated)
Study Completion Date
March 15, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Taiwan University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
In a prospective study investigating the prevalence of STIs among at-risk PLWH, the prevalence of Chlamydia trachomatis and N. gonorrhoeae was 24.7% and 12.1%, respectively. Surprisingly, the study found high rates of C. trachomatis and/or N. gonorrhoeae co-infections in PLWH with recent hepatitis C virus (HCV) infection (50%), HBsAg positivity (44%), and early syphilis (36%). Considering the high rate of sexually transmitted co-infections, combination therapy of single-dose ceftriaxone plus 7-day doxycycline for early syphilis may provide convenience and benefit to treatment of N. gonorrhoeae and C. trachomatis co-infections at a single clinic encounter. In the present study, this study aim to compare the efficacy of ceftriaxone plus doxycycline versus BPG plus doxycycline as the treatment for early syphilis among PLWH.
Detailed Description
Enrolled criteria: PLWH aged 20 years or more PLWH with early syphilis (i.e. primary, secondary, or early latent syphilis), confirmed by a positive rapid plasma reagin (RPR) titer with a reactive Treponema pallidum particle agglutination (TPPA) assay. PLWH has provided informed consent *A participant with repeated syphilis can be repeated enrolled after signing an informed consent if the previous episode of early syphilis was successfully treated with achieving at least a 4-fold decrease in RPR titers and 48-week follow-up is completed. Exclusion criteria: PLWH with RPR titers of less than 4 Exposure to antibiotics with activity against T. pallidum, such as penicillins, third-generation cephems, doxycycline, or macrolides, within the preceding 4 weeks A known or suspected infection other than syphilis requiring additional treatment with an antimicrobial active against T. pallidum A history of intolerance to penicillin, ceftriaxone, or doxycycline Pregnancy Primary outcome: Serologic response at month 6 (defined as either a 4-fold or greater decline in RPR titer compared to baseline or being RPR-nonreactive) Secondary outcomes: Microbiologic response of syphilis (defined as T. pallidum PCR Ct value >38) at week 4 Microbiologic response of bacterial STIs (defined as negative PCR results) at week 4 Serologic response at months 3 and 12 Safety of study treatment recorded by using a diary (all adverse events will be coded and graded according to Common Terminology Criteria for Adverse Events [CTCAE] v4.0.) Adherence evaluation (the noting of tablet intake in the diary for the 7 days of the treatment period)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Early Syphilis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
single-dose ceftriaxone plus doxycycline
Arm Type
Active Comparator
Arm Description
single-dose ceftriaxone (1g intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)
Arm Title
single-dose BPG plus doxycycline
Arm Type
Active Comparator
Arm Description
single-dose BPG (2.4 MU intramuscularly once) plus doxycycline (100 mg orally twice daily for 7 days)
Intervention Type
Drug
Intervention Name(s)
Doxycycline
Intervention Description
doxycycline (100 mg orally twice daily for 7 days)
Intervention Type
Drug
Intervention Name(s)
Ceftriaxone
Intervention Description
Ceftriaxone (1g intramuscularly once)
Intervention Type
Drug
Intervention Name(s)
benzathine penicillin G
Intervention Description
benzathine penicillin G (2.4 MU intramuscularly once)
Primary Outcome Measure Information:
Title
Rate of serologic response at month 6
Description
Serologic response is defined as either a 4-fold or greater decline in RPR titer compared to baseline or being RPR-nonreactive
Time Frame
Month 6
Secondary Outcome Measure Information:
Title
Rate of microbiologic response of syphilis at week 4
Description
Microbiologic response of syphilis is defined as T. pallidum PCR Ct value >38
Time Frame
Week 4
Title
Rate of microbiologic response of bacterial STIs at week 4
Description
Microbiologic response of bacterial STIs is defined as negative PCR results
Time Frame
Week 4
Title
Rate of serologic response at months 3 and 12
Description
Serologic response is defined as either a 4-fold or greater decline in RPR titer compared to baseline or being RPR-nonreactive
Time Frame
Months 3 and 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PLWH aged 20 years or more PLWH with early syphilis (i.e. primary, secondary, or early latent syphilis), confirmed by a positive rapid plasma reagin (RPR) titer with a reactive Treponema pallidum particle agglutination (TPPA) assay. PLWH has provided informed consent Exclusion Criteria: PLWH with RPR titers of less than 4 Exposure to antibiotics with activity against T. pallidum, such as penicillins, third- generation cephems, doxycycline, or macrolides, within the preceding 4 weeks A known or suspected infection other than syphilis requiring additional treatment with an antimicrobial active against T. pallidum A history of intolerance to penicillin, ceftriaxone, or doxycycline Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kuan-Yin Lin
Phone
+886975607715
Email
kuanyin0828@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kuan-Yin Lin
Organizational Affiliation
National Taiwan University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kuan-Yin Lin
City
Taipei
ZIP/Postal Code
110
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kuan-Yin Lin
Phone
+886975607715
Email
maregold@ntuh.gov.tw

12. IPD Sharing Statement

Plan to Share IPD
No

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Treatment Responses of Early Syphilis to Ceftriaxone Plus Doxycycline

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