Trial · NCT03795194
Antibiotic Duration in Post-appendectomy Abscess
NCT03795194, Phase 4, Terminated, Phoenix Children's Hospital; results first posted 2024-03-08
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Antibiotic Duration in Post-appendectomy Abscess. Trials, record NCT03795194. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03795194
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Antibiotic Duration in Post-appendectomy Abscess
- NCT number
- NCT03795194
- Status
- Terminated
- Phases
- Phase 4
- Enrollment
- 7 participants, actual
- Lead sponsor
- Phoenix Children's Hospital
- Conditions
- Complicated Appendicitis, Perforated Appendicitis
- Interventions
- ampicillin/clavulanate
- First posted
- 2019-01-07
- Last updated
- 2024-03-08
- Results first posted
- 2024-03-08
- Limitations and caveats
- Low enrollment. Early termination leading to small number of subjects analyzed.
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Hospital Readmission Rate | 30 days | Rate of readmission to the hospital after abscess drainage. |
| Primary | Length of Hospital Stay | 30 days | How many days patient stays in the hospital if and when they are readmitted after their abscess drainage. |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Hospital Readmission Rate | 30 days | Participants | COUNT_OF_PARTICIPANTS | |
| PRIMARY | Length of Hospital Stay | 30 days | Participants were not readmitted to the hospital after abscess drainage. |
Source ClinicalTrials.gov
Results by group2
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Hospital Readmission Rate | Arm A (8-Day) 30-day Readmission Rate | 0 | Participants | ||
| Hospital Readmission Rate | Arm B (4-Day) 30-day Readmission Rate | 0 | Participants |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | 8-day | 3 | |
| Overall Study | STARTED | 4-day | 4 | |
| Overall Study | COMPLETED | 8-day | 3 | |
| Overall Study | COMPLETED | 4-day | 4 | |
| Overall Study | NOT COMPLETED | 8-day | 0 | |
| Overall Study | NOT COMPLETED | 4-day | 0 |
Source ClinicalTrials.gov
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 totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | 8-day | 0 | 3 |
| Total, all-cause mortality | 4-day | 0 | 4 |
| Total, other adverse events | 8-day | 0 | 3 |
| Total, other adverse events | 4-day | 0 | 4 |
| Total, serious adverse events | 8-day | 0 | 3 |
| Total, serious adverse events | 4-day | 0 | 4 |
Source ClinicalTrials.gov
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 comparisons3
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Arm A (8-Day) 30-day Readmission Rate vs Arm B (4-Day) 30-day Readmission Rate: Hospital Readmission Rate | Trial comparisons |
| 8-day vs 4-day: deaths from any cause | Trial comparisons |
| 8-day vs 4-day: serious adverse events | Trial comparisons |
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/NCT03795194
GET https://conductscience.org/api/trials/v1/NCT03795194/registered