Trial · NCT06027593
Outcomes28
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
1 to 20 of 28
Download this page as JSON| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Guideline-concordant Antibiotic Use for Adults With Pharyngitis | Pre-intervention and post-intervention, up to 2 years | Data for adults with pharyngitis only | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Guideline-concordant Antibiotic Use for Children With Acute Otitis Media | Pre-intervention and post-intervention, up to 2 years | Note: this metric of guideline-concordant antibiotic use was measured using a denominator of those who were prescribed antibiotics (pre-intervention: 9,020 participants; post-intervention: 7,778 participants). The overall number of participants with acute otitis media (pre-intervention: 10,167 participants; post-intervention: 8,741 participants) was NOT used as the denominator for this reason. | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Guideline-concordant Antibiotic Use for Adults With Community-acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for adults with community-acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| PRIMARY | Guideline-concordant Antibiotic Use for Children With Community-acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for children with community-acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Choice for Adults Hospitalized With Community Acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for adults hospitalized with community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Duration for Adults Hospitalized With Community Acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for adults hospitalized with community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 30-day Community Acquired Pneumonia-related Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Adults | 30 days | Data for adults with community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 30-day Readmissions for Community Acquired Pneumonia in Adults | 30 days | Data for adults with community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Choice for Pediatric Community Acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for pediatric community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Duration for Pediatric Community Acquired Pneumonia | Pre-intervention and post-intervention, up to 2 years | Data for pediatric community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 28-day Community Acquired Pneumonia-related Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Children | 28 days | Data for pediatric community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 28-day Readmissions for Pediatric Community Acquired Pneumonia | 28 days | Data for pediatric community acquired pneumonia only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Decision to Prescribe Antibiotics for Adult Pharyngitis | Pre-intervention and post-intervention, up to 2 years | This metric encapsulates patients who did and did not receive antibiotics. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Choice Adult Pharyngitis | Pre-intervention and post-intervention, up to 2 years | Note: this metric of guideline-concordant antibiotic use was measured using a denominator of those who were prescribed antibiotics for adult pharyngitis (pre-intervention: 32 participants; post-intervention: 175 participants). The overall number of participants with adult pharyngitis (pre-intervention: 2,032 participants; post-intervention: 3,764 participants) was NOT used as the denominator for this reason. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Duration for Adult Pharyngitis | Pre-intervention and post-intervention, up to 2 years | Note: this metric of guideline-concordant antibiotic use was measured using a denominator of those who were prescribed antibiotics for adult pharyngitis (pre-intervention: 32 participants; post-intervention: 175 participants). The overall number of participants with adult pharyngitis (pre-intervention: 2,032 participants; post-intervention: 3,764 participants) was NOT used as the denominator for this reason. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 30-day Pharyngitis Outpatient Revisits (Emergency Department, Urgent Care, or Primary Care) in Adults | 30 days | Data for Adult Pharyngitis only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | 30-day Deep Neck Space Infection Admission | 30 days | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Guideline-concordant Decision to Prescribe Antibiotics for Pediatric Acute Otitis Media | Pre-intervention and post-intervention, up to 2 years | This metric encapsulates patients who did and did not receive antibiotics. | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Choice for Pediatric Acute Otitis Media | Pre-intervention and post-intervention, up to 2 years | Data for pediatric acute otitis media only | Participants | COUNT_OF_PARTICIPANTS |
| SECONDARY | Guideline-concordant Antibiotic Duration for Pediatric Acute Otitis Media | Pre-intervention and post-intervention, up to 2 years | Data for pediatric acute otitis media only | Participants | COUNT_OF_PARTICIPANTS |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this list from software.
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GET https://conductscience.org/api/trials/v1/NCT06027593/outcomes