Congenital Syphilis Clinical Trials

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Comprehensive Ambulatory Antibiotics for the Treatment of Congenital Syphilis

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

CARES-1 is a randomised, open-label, phase II pharmacokinetic (PK) and safety study of ambulatory antibiotics for the treatment of neonates with all-risk asymptomatic congenital syphilis.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 7 days
Healthy Volunteers: f
View:

• Infants at risk of congenital syphilis at birth defined as:

‣ an infant born to a mother who tests positive for syphilis in pregnancy using registered and licensed locally-available diagnostic tests for example but not limited to a Treponemal rapid POCT, an RPR or both.

‣ AND

⁃ the mother is untreated in the current pregnancy defined as:

• i. she tested positive at antenatal care and received no treatment OR ii. she was never tested during antenatal care OR iii. she tested negative at antenatal care and positive on re-testing at delivery

• OR c. the mother is inadequately treated in the current pregnancy defined as:

• i. Having received a non-penicillin based treatment regimen; and/or ii. Does not have documentation of 3 doses of IM Benzathine Penicillin, given 7-10 days apart, with the last dose given \> 30 days prior to delivery OR b. The mother was adequately treated in the current pregnancy BUT considers herself at risk of re-infection following a midwife delivered explanation of risk (partner treatment, multiple partners etc).

• Infants who are asymptomatic for a diagnosis of congenital syphilis following application of a clinical proforma by the study team (Appendix 1)

• Infants who are less than \<= 7 days of life AND with a post-menstrual age (PMA) of 34-42 weeks (Appendix 2).

• Infants who are tolerating enteral feeds, including if they are being administered by an NG tube.

Locations
Other Locations
Indonesia
Universitas Indonesia
NOT_YET_RECRUITING
Jakarta
Malawi
Malawi Liverpool Wellcome Programme
NOT_YET_RECRUITING
Blantyre
South Africa
Stellenbosch
RECRUITING
Stellenbosch
Contact Information
Primary
Sarah Prentice
sarah.prentice@lshtm.ac.uk
+4420 7636 8636
Time Frame
Start Date: 2026-05-04
Estimated Completion Date: 2027-06-30
Participants
Target number of participants: 90
Treatments
Experimental: Oral Linezolid
10 day course of Linezolid twice a day
Experimental: Oral Amoxicillin
10 day course of Amoxicillin twice a day
Active_comparator: IM Benzathine penicillin
Single IM dose of IM Benzathine penicillin
Related Therapeutic Areas
Sponsors
Collaborators: PHPT/AMS Laboratory, Faculty of Associated Medical Sciences, Chiang Mai University, Murdoch Childrens Research Institute, Malawi Liverpool Wellcome Programme, University of Stellenbosch, MRC CTU at UCL, University of Sydney, University College Dublin
Leads: London School of Hygiene and Tropical Medicine

This content was sourced from clinicaltrials.gov

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