Phase
Condition
Hiv
Sexually Transmitted Diseases (Stds)
Gynecological Infections
Treatment
BPG
Doxycycline
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients aged ≥ 18 years
Patients who, after the nature of the study has been explained to them, and beforeany protocol-specific procedures are performed, give informed consent in writing, inaccordance with local regulatory requirements
Patients with or without HIV infection and with syphilis infection in the earlystages according to CDC criteria (primary syphilis, secondary syphilis and earlylatent syphilis of less than one year's duration)
Patients with a positive non-treponemal assay result
Patients available for participation and follow-up during the 6 months of the study
Patients covered by the French health insurance system
Exclusion
Exclusion Criteria:
Individuals with a history of known hypersensitivity to doxycycline or any otherantibiotic of the tetracycline family, BPG (hypersensitivity to the active substancebenzathine benzylpenicillin, to other penicillins, to soy phospholipids, peanuts orany of the excipients in the product ; history of severe immediate hypersensitivityreactions (eg anaphylaxis) to other beta-lactams (examples: cephalosporins,carbapenemes or monobactams), lidocaïne (hypersensitivity to lidocainehydrochloride, amide-linked local anesthetics, or any of the excipients listed inSPC) and / or any of the excipients of the specialties used in the study
Patients with a negative non-treponemal assay result
Patients receiving an anticoagulant therapy
Individuals with contraindications for either of the study drugs
Individuals treated with retinoids by general route
Individuals with early and late neurosyphilis
Individuals requiring doxycycline treatment
Individuals with late syphilis, whether or not latent (e.g. cutaneous)
Individuals with thrombocytopenia or coagulation disorders contraindicatingintramuscular injections
Women who are pregnant or breast-feeding, or of childbearing age not using orplanning to use acceptable birth control measures;
Individuals under a measure of legal protection or unable to consent
Individuals participating in any clinical trial with another investigational productin the 28 days preceding the first study visit or intending to participate inanother clinical study at any time during the course of this study.
Recent exposure
Study Design
Connect with a study center
CHRU Jean Minjoz
Besancon, 25000
FranceActive - Recruiting
Hôpital Henri Mondor
Créteil, 94000
FranceActive - Recruiting
Hôpital de la Croix Rousse
Lyon, 69000
FranceActive - Recruiting
Hôpital Cochin
Paris, 75014
FranceActive - Recruiting
Hôpital Hotel Dieu
Paris, 75001
FranceActive - Recruiting
Hôpital Saint Louis - GeGIDD
Paris, 75009
FranceActive - Recruiting
Hôpital Saint Louis - SMIT
Paris, 75009
FranceActive - Recruiting
CHU Toulouse - Hôpital de la Grave - GeGIDD
Toulouse, 34000
FranceActive - Recruiting
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