Skip to content

Clinical efficacy of penicillin or ceftriaxone in the treatment of neurosyphilis and its influencing factors

Clinical efficacy of penicillin or ceftriaxone in the treatment of neurosyphilis and its influencing factors

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047164
Enrollment
Unknown
Registered
2021-06-09
Start date
2021-11-30
Completion date
Unknown
Last updated
2023-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Syphilis

Interventions

Group1:treatment with aqueous crystalline penicillin G
Group2:treatment with ceftriaxone

Sponsors

Institute of Dermatology, Chinese Academy of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Randomized enrolment of first-diagnosed neurosyphilis patients (untreated patients referred from other hospitals could also be included); 2. Aged 18 to 75 years; 3. No intravenous or intramuscular injection of antibiotics for treatment of neurosyphilis for the last 3 months. (ACPG, ceftriaxone, procaine penicillin G, etc.); 4. The diagnosis of neurosyphilis should meet the following criteria: (1) History of syphilis infection at any stage; (2) With or without central nervous system manifestations; (3) Laboratory findings: abnormal cerebrospinal fluid (CSF) routine test: elevated white blood cell count: >=5 cells /mL (combined with HIV-infected: > 20 cells /mL) or protein concentration of > 500 mg/L (excluding other diseases that may be affected) and meeting one or more of the following findings reactive CSF VDRL or FTA-ABS test; reactive CSF TPPA or RPR/TRUST tests; 5. Patients voluntarily signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergic to the ACPG/ceftriaxone. 2. Patients were excluded from other central nervous system diseases or conditions that might cause abnormalities in CSF tests. 3. Pregnant and lactating women. 4. Patients had serious adverse reactions during treatment. 5. The standardized treatment is not carried out strictly according to the treatment regimen; or were unable to follow up as required. 6. Patients require termination of treatment, and the efficacy and adverse reactions cannot be evaluated; or request withdrawal from the study. 7. Patients with incomplete clinical data that cannot be counted.

Design outcomes

Primary

MeasureTime frame
CSF white blood cell count;Serum RPR titer;CSF RPR/VDRL titer;MMSE score;

Secondary

MeasureTime frame
Cerebrospinal fluid protein levels;

Countries

China

Contacts

Public ContactWang Qianqiu

Institute of Dermatology, Chinese Academy of Medical Science

wangqianqiunj@126.com+86 139 5192 1995

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026