Trial · NCT04083417
Sore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and No Antibiotic Treatment
NCT04083417, Phase 4, Recruiting, Katarina Hedin
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Sore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and No Antibiotic Treatment. Trials, record NCT04083417. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04083417
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Sore Throat in Primary Care - a Comparison of Phenoxymethylpenicillin and No Antibiotic Treatment
- NCT number
- NCT04083417
- Status
- Recruiting
- Phases
- Phase 4
- Enrollment
- 260 participants, estimated
- Lead sponsor
- Katarina Hedin
- Conditions
- Sore Throat, Tonsillitis
- Interventions
- Phenoxymethylpenicillin, No antibiotic treatment
- First posted
- 2019-09-10
- Last updated
- 2024-12-04
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Differences in number of days from inclusion to resolution of symptoms | 10 days after inclusion | Differences between the randomized groups. Symptom resolution is defined as the first day the item sore throat and difficulty swallowing is scored less than moderately bad |
| Secondary | Proportions of patients with symptom resolution at each of the days 2 through 10. | up to 10 days after inclusion | |
| Secondary | The number of days from inclusion to symptom resolution of the individual items of sore throat symptoms. | 10 days after inclusion | |
| Secondary | Differences in number of days from inclusion to the day the patient can put up with the pain. | up to 10 days after inclusion | |
| Secondary | The possible change in the self-reported items of symptoms on the rating scale for each of the days 2 through 10 and describe the break through day for improvement | up to between 10 days after inclusion | The rating is on a 7-point Likert scale 0=no symptoms, 1= very little, 2=slight, 3=moderately bad, 4=bad, 5=very bad, 6=as bad as it could be. |
| Secondary | The number of days the patient needs to stay at home from work/school | 10 days after inclusion | |
| Secondary | Proportion of patients with future episodes of sore throat | 30 days and 3 months after inclusion | |
| Secondary | Proportion of patients at follow up with eradication of each of the potential pathogens found. | between 18 up to 24 days | Bacteriological eradication |
| Secondary | The number of adverse events | 3 months after inclusion | |
| Secondary | Description of patient characteristics and outcomes in the drop-out group. | 3 months |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license 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 trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04083417
GET https://conductscience.org/api/trials/v1/NCT04083417/registered