Recruiting

Amoxicillin-Clavulanate

Sponsor:

University of Missouri-Columbia

Code:

NCT05846399

Conditions

Cat Bite

Hand Injuries

Arm Injury

Infection, Bacterial

Anti-bacterial Agents

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Amoxicillin/clavulanate

Ciprofloxacin

Clindamycin

Placebo (microcrystalline cellulose)

Wound management

Study Details

Brief summary:

Cat bites are puncture wounds that have the potential to seed bacteria deep within the joint capsule, periosteum, and bone. The hand is the most common site of bite injuries. Pasteurella multocida is the is the most common organism isolated from the mouths of cats that can cause infections after a bite. Prophylactic antibiotics are often recommended with amoxicillin-clavulanate for 3-5 days to decrease the incidence of developing an infection. However, only one randomized controlled clinical trial consisting of 12 patients has been performed to justify this course of treatment, raising the possibility that the use of antibiotics could be reduced or even eliminated. Investigators will compare different durations of prophylactic antibiotics and a placebo control for cat bites to the hand/forearm presenting to the Emergency Department, Urgent Care, Plastic Surgery Clinic using a randomized, controlled, double-blind clinical trial. Participants presenting to the University of Missouri Hospital Emergency Department, Missouri University (MU) Healthcare Urgent Care, Plastic Surgery Clinic over the next year will be offered the chance to enroll if they meet the inclusion/exclusion criteria. For inclusion, participants will be >18 years of age, have cat bites to the hand or distal to elbow, and present within 24 hours of the cat bite injury. Participants must not present with active local or systemic infections, have received antibiotics within the past 30 days, or be immunocompromised (primary and secondary immunodeficiencies). Participants will be randomized to one of three treatment arms (placebo; amoxicillin-clavulanate 1 day; amoxicillin-clavulanate 5 days). Outcomes are the development of an infection at the location of the cat bite and/or systemic infection, adverse effects of interventions, disability assessed by Quick Disabilities of Arm, Shoulder and Hand (QuickDASH) scores, and quality of life (QOL) assessed by HAND Questionnaire (HAND-Q) scores. Infection will be assessed at day 0, day 2, day 7+/-2, day 14+/-2, and day 30+/-2 by vital signs, laboratory values, physical examination and with an infrared and digital camera. All measures will be within the standard of care, apart from the infrared camera, QuickDASH, and HAND-Q scores. The anatomic locations of cat bites to the hand/forearm will be assessed for correlations with infections.

Conditions

Cat Bite

Hand Injuries

Arm Injury

Infection, Bacterial

Anti-bacterial Agents

Study ID

NCT05846399

Start date

Sep 7, 2023

Status verified date

Oct, 2025

Completion date

Aug 1, 2027

Anticipated

Primary completion date

Jul 1, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Patients greater or equal to 18 years of age.
  • Bitten by a cat.
  • Location of bite is the hand and/or forearm (distal to elbow).
  • Presenting <24 hours following a cat bite to the hand/forearm.
  • English speaking

Exclusion Criteria:

  • Patients who present with active local or systemic infections

1. Purulent drainage from the cat bite
2. Redness AND swelling at the location of the cat bite
  • Having a fever >100.4° F or >38° C)-Received antibiotics within the past 30 days
  • Received antibiotics within the past 30 days
  • Patients unwilling to take study medication
  • Patients unwilling to attend scheduled follow-up evaluations or complete study forms
  • Pregnant Women
  • Type I hypersensitivity reaction to any of the study interventions
  • Immunocompromised patients (primary and secondary immunodeficiencies) Primary
  • Autoimmune Lymphoproliferative Syndrome (ALPS)
  • Autoimmune Polyglandular Syndrome type 1 (APS-1)
  • B-cell Expansion with Nuclear factor kappa-light-chain-enhancer of activated B cells and T-cell Anergy (BENTA) Disease
  • Caspase Eight Deficiency State (CEDS)
  • Caspase Recruitment Domain Family Member 9 (CARD9) Deficiency and Other Syndromes of Susceptibility to Candidiasis
  • Cartilage-hair hypoplasia
  • Chédiak-Higashi syndrome
  • Chronic Granulomatous Disease (CGD)
  • Common Variable Immunodeficiency (CVID)
  • Complement Deficiencies
  • Congenital Neutropenia Syndromes
  • Cytotoxic T-Lymphocyte Associated Protein 4 (CTLA4) Deficiency
  • Cyclic neutropenia
  • DiGeorge syndrome
  • Dedicator Of Cytokinesis 8 (DOCK8) Deficiency
  • GATA-binding protein 2 (GATA2) Deficiency
  • Glycosylation Disorders with Immunodeficiency
  • Hyper-Immunoglobulin E Syndromes (HIES)
  • Hyper-Immunoglobulin M Syndromes
  • Interferon Gamma, Interleukin 12 and Interleukin 23 Deficiencies
  • Leukocyte Adhesion Deficiency (LAD) Types 1 and 2
  • Lipopolysaccharide Responsive Beige-Like Anchor Protein (LRBA) Deficiency
  • Phosphatidylinositol 3-kinase (PI3-Kinase) Disease
  • Phospholipase C gamma 2 (PLCG2) associated Antibody Deficiency and Immune Dysregulation (PLAID)
  • Severe Combined Immunodeficiency (SCID)
  • Selective Immunoglobulin A (IgA) deficiency
  • Signal transducer and activator of transcription 3 (STAT3) Dominant-Negative Disease
  • STAT3 Gain-of-Function Disease
  • Warts, Hypogammaglobulinemia, Infections, and Myelokathexis (WHIM) Syndrome
  • Wiskott-Aldrich Syndrome (WAS)
  • X-Linked Agammaglobulinemia (XLA)
  • X-Linked Lymphoproliferative Disease (XLP)
  • X-linked magnesium transporter 1 (MAGT1) deficiency with increased susceptibility to Epstein-Barr virus (EBV) infection and N-linked glycosylation defect (XMEN) Disease
  • Zeta-associated protein 70 (ZAP-70) deficiency

Secondary

  • Malnutrition
  • Uncontrolled Diabetes mellitus
  • Chronic uremia
  • Genetic syndromes: trisomy 21
  • Immunomodulatory, immunosuppressive drug therapy: corticosteroids, calcineurin inhibitors, cytotoxic agents
  • Systemic lupus erythematosus
  • Malignancy
  • Active radiation therapy
  • Bone marrow ablation
  • Infectious diseases: human immunodeficiency virus (HIV) infection, Hepatitis

Additional Primary and secondary immunodeficiencies can be found at the following link.

https://www.merckmanuals.com/professional/immunology-allergic-disorders/immunodeficiency-disorders/overview-of-immunodeficiency-disorders

Study Design

Enrollment

72 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Prevention

Interventions and Outcome Measures

Arms

placebo comparator: Placebo (microcrystalline cellulose)

Placebo capsules by mouth twice daily x 5 days (5 days of placebo microcrystalline cellulose capsules)

active comparator: Antibiotic x 1 day

Amoxicillin-clavulanate 875-125mg capsules by mouth twice daily x 1 day (4 days of placebo capsules)

-Penicillin allergy: ciprofloxacin 500mg by mouth twice daily + clindamycin 300mg by mouth three times daily x 1 day

active comparator: Antibiotic x 5 days

Amoxicillin-clavulanate 875-125mg capsules by mouth twice daily x 5 days (0 days of placebo capsules)

-Penicillin allergy: ciprofloxacin 500mg by mouth twice daily + clindamycin 300mg by mouth three times daily x 5 days

Interventions

Amoxicillin/clavulanate

Amoxicillin-clavulanate 875-125mg by mouth twice daily for 1 day or Ciprofloxacin 500mg by mouth twice daily and clindamycin 450mg by mouth twice daily for 1 day

Ciprofloxacin

Amoxicillin-clavulanate 875-125mg by mouth twice daily for 5 days or Ciprofloxacin 500mg by mouth twice daily and clindamycin 450mg by mouth twice daily for 5 days

Clindamycin

Amoxicillin-clavulanate 875-125mg by mouth twice daily for 5 days or Ciprofloxacin 500mg by mouth twice daily and clindamycin 450mg by mouth twice daily for 5 days

Placebo (microcrystalline cellulose)

Placebo (microcrystalline cellulose) by mouth twice daily by mouth for 5 days

Wound management

Wound management includes hemostasis, copious irrigation, removal of foreign bodies, and excisional debridement of devitalized tissue. If only punctures are present, lancing of the punctures is not typically required unless infection has already developed. Local anesthesia (1% lidocaine hydrogen chloride (HCl) with epinephrine 1:100,000; 200mg/20mL vial) will be used prior to irrigation (30mL of povidone-iodine in 1L of 0.9% sodium chloride (NaCl) solution and/or 118mL of 3% hydrogen peroxide) and debridement. Open wounds will be irrigated and debrided at bedside. Wounds will be covered with soft dressings in place until first follow-up at day 2.

Primary outcome measure

  • Incidence of infection [ Time Frame: Day 30+/-2 ]
  • Changes of the incidence of infection [ Time Frame: Day 2; Day 7+/-2; Day 14+/-2; Day 30+/-2 ]

Central Contacts and Locations

Central contacts

Locations

University of Missouri

Recruiting

Columbia, Missouri, United States, 65212

Contacts

More Information

Sponsor

University of Missouri-Columbia

Last update posted

Oct 15, 2025

Last verified

Oct, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by University of Missouri-Columbia on 2025-10-15.