Comparative Effectiveness of Available Treatments for Sinus and Ear Infections in Children (Acute Sinusitis)

Part of paid clinical trials in Denver, Colorado.

Sponsor
Nader Shaikh
Study ID
NCT07732699
Phase
PHASE4
Status
Not Yet Recruiting

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Conditions

  • ACUTE SINUSITIS
  • Sinusitis

Eligibility Criteria

Sex
ALL
Age
2 Years - 12 Years
Healthy Volunteers
Not accepted

Interventions

  • Amoxicillin — DRUG
    Amoxicillin administered orally at protocol-specified, weight-based dosing consistent with standard pediatric treatment guidelines for AS, for the defined treatment duration.
  • Amoxi Clavulanate — DRUG
    Amoxicillin-clavulanate administered orally at protocol-specified, weight-based dosing consistent with standard pediatric treatment guidelines for AOM or AS, for the defined treatment duration.
  • Amoxicillin Placebo — DRUG
    Matching placebo administered orally according to the same dosing schedule and treatment duration as the active comparator arms
  • Amoxicillin-Clavulanate Placebo — DRUG
    Matching placebo administered orally according to the same dosing schedule and treatment duration as the active comparator arms.

Study Details

This study is being conducted at multiple hospitals and clinics to better understand whether antibiotics truly help children feel better when they have a sinus infection (acute sinusitis). Children in the study are randomly assigned (like flipping a coin) to receive either amoxicillin, amoxicillin-clavulanate, or a placebo (a look-alike medicine with no active antibiotic). Neither families nor study staff know which treatment the child is receiving during the study. The main goal is to compare how severe children's symptoms are each day while on these treatments. Parents or caregivers will report symptoms daily using a simple electronic diary. The study will also examine whether factors such as the severity of the child's illness or signs of allergies affect how well antibiotics work. The results will help guide better treatment decisions for children with sinus infections.

Key Dates

First listed
Jul 29, 2026
Start date
Oct 1, 2026
Status verified
Jul 2026
Primary completion
Dec 18, 2031
Completion
Mar 17, 2032

Study Design

Enrollment
1,100 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Active Comparator: Amoxicillin
    Participants randomized to this arm will receive oral amoxicillin for the treatment of acute sinusitis (AS). Caregivers will complete daily electronic symptom diaries throughout the treatment period.
  • Active Comparator: Amoxicillin-Clavulanate
    Participants randomized to this arm will receive oral amoxicillin-clavulanate for the treatment of AS. Caregivers will complete daily electronic symptom diaries throughout the treatment period.
  • Placebo Comparator: Amoxicillin Placebo
    Participants randomized to this arm will receive a matching oral placebo for the treatment of AS. Caregivers will complete daily electronic symptom diaries throughout the treatment period.
  • Placebo Comparator: Amoxicillin-Clavulanate Placebo
    Participants randomized to this arm will receive a matching oral placebo for the treatment of AS. Caregivers will complete daily electronic symptom diaries throughout the treatment period.

Primary Outcome Measure

Average Daily Symptom Burden [ Time Frame: Days 1-10 ]

Central Contacts

Locations (5)

FacilityCityStateZIPSite coordinators
University of Colorado, DenverDenverColorado80204
Sean O'Leary, MD
303-724-1582
Duke University HospitalDurhamNorth Carolina27705
Charles Wood, MD
919-620-4772
Cincinnati Children's HospitalCincinnatiOhio45229
Bill Brinkman, MD
513-636-2576
UPMC Children's Hospital of PittsburghPittsburghPennsylvania15213
Nader Shaikh, MD
412-692-8111
Seattle Children's HospitalSeattleWashington98105
Douglas Opel, MD
206-987-6894

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