Comparing Optimal Step-down Therapy for Children With Invasive MRSA Trimethoprim-Sulfamethoxazole vs. Clindamycin for the Treatment of Children With Invasive MRSA Infections

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

The goal of this clinical trial is to learn if trimethoprim-sulfamethoxazole (TMP-SMX) works to treat invasive infections due to methicillin-resistant Staphylococcus aureus (MRSA) in children. It will also learn about the safety of TMP-SMX in the treatment of children with invasive MRSA infections. The main questions it aims to answer are: -Is TMP-SMX effective at successfully treating children with invasive infections due to MRSA? What are the side effects of TMP-SMX in children taking it for invasive infections due to MRSA? Researchers will compare TMP-SMX to a clindamycin (a commonly prescribed antibiotic for the treatment of MRSA in children) to see if TMP-SMX works better, worse or the same as clindamycin for children with invasive infections due to MRSA. Participants will: Take TMP-SMX or clindamycin for the treatment of their invasive infection due to MRSA. Will follow up with the provider treating their invasive infection at the discretion of the treating provider. Keep a diary of their symptoms and any side effects of the medicine

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2 months
Maximum Age: 18
Healthy Volunteers: f
View:

• 60 days to 18 years of age (inclusive) at the time of oral step down treatment

• Diagnosed by the clinical team with OAI or HNI:

‣ OAI- at least 1 focal finding and 1 systemic finding OR radiographic confirmation of OAI

• Focal finding- pain/swelling over a bone/joint, or restricted movement/failure to bear weight

∙ Systemic finding- fever \>38oC, or elevated c-reactive protein (CRP) or elevated erythrocyte sedimentation rate. (ESR) or elevated white blood cell count (WBC) or elevated WBC in synovial fluid OR

∙ Radiographic confirmation- findings consistent with osteomyelitis or septic arthritis - Plain radiograph, MRI, CT or ultrasound, bone scan result indicating abnormal bone, subperiosteal or bone marrow findings consistent with infection

⁃ HNI- at least 1 focal finding and 1 systemic finding OR radiographic confirmation of HNI

• Focal finding- facial pain or redness, eye pain or proptosis, neck or throat pain or swelling, ear pain or proptosis

∙ Systemic finding- fever \>38oC, or elevated CRP or elevated ESR or elevated WBC OR

∙ Radiographic confirmation- findings consistent with facial/orbital cellulitis, cervical lymphadenitis, mastoiditis, or deep neck infection/abscess (including peritonsillar, retro- and para-pharyngeal. Plain radiograph, MRI, CT or ultrasound, bone scan result indicating abnormal findings consistent with infection

• Treated by the clinical team for confirmed MRSA or suspected MRSA infection

‣ Confirmed MRSA- positive culture for MRSA from a sterile body fluid (e.g., blood, abscess, bone, synovial fluid, or other surgical specimen)

⁃ Suspected MRSA- treatment for MRSA by the clinical team without microbiologic confirmation (e.g., negative cultures)

• Currently ready or planned to be transitioned to oral antibiotic therapy by the clinical team

• OAI or HNI symptoms \< 14 days at the time of hospital admission

Locations
United States
Indiana
Riley Hospital for Children
RECRUITING
Indianapolis
Contact Information
Primary
Mary Stumpf
mestumpf@iu.edu
317-274-8801
Time Frame
Start Date: 2025-05-20
Estimated Completion Date: 2027-06
Participants
Target number of participants: 100
Treatments
Experimental: TMP-SMX
Trimethoprim-sulfamethoxazole~* For osteoarticular infections- 4-5 mg/kg/dose (based on TMP) PO every 8 hours (max dose 320mg/dose)~* For head and neck infections- 5-6 mg/kg/dose (based on TMP PO every 12 hours (max dose 320mg/dose)~Duration will be at the discretion of the treating provider
Active_comparator: Clindamycin
13 mg/kg/dose PO every 8 hours (max 600mg/dose) Duration will be at the discretion of the treating provider
Sponsors
Leads: Indiana University

This content was sourced from clinicaltrials.gov