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Study of Cefditoren Pivoxil in Treatment of Childhood With Acute Rhinosinusitis

A Comparison of Cefditoren Pivoxil 10 mg/kg/Day and Cefditoren Pivoxil 20 mg/kg/Day in Treatment of Childhood With Acute Rhinosinusitis

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01553006
Acronym
RS
Enrollment
120
Registered
2012-03-13
Start date
2012-01-31
Completion date
2012-09-30
Last updated
2012-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rhinosinusitis

Keywords

rhinosinusitis, cefditoren pivoxil

Brief summary

Cefditoren pivoxil has been used in rhinosinusitis treatment. However, little is known about the efficacy of this drug at low and high doses.

Detailed description

The investigation was a randomized, investigator-blinded, and parallel study, conducted in patients (age 1-15 years) with acute rhinosinusitis. Two groups of patients were randomized received low (10 MKD) or high (20 MKD) of drug for 14 days. Changes in sinus symptoms scores, response rate and adverse effect were evaluated at days 7 and 14. Relapse rate was recorded at days 21 and 28. Recurrence of sinus symptoms at day 60 were assessed.

Interventions

comparison of different dosages of cefditoren pivoxil

Sponsors

Thammasat University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
1 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* children age 1-15 years old diagnosed acute rhinosinusitis

Exclusion criteria

* poor compliance * other infections

Design outcomes

Primary

MeasureTime frameDescription
sinus symptoms scores14 daysChange of sinus sympotms scores from baseline in 2 weeks

Secondary

MeasureTime frameDescription
relapse rateat day 28The relapse rate of sinus symptoms scores at day 28.

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026