Trial · NCT00822692
Trial of Septra for Uncomplicated Skin Abscesses in Patients at Risk for Community Acquired Methicillin-Resistant Staphylococcus Aureus Infection
NCT00822692, Not applicable, Completed, 59th Medical Wing; results first posted 2009-09-03
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Trial of Septra for Uncomplicated Skin Abscesses in Patients at Risk for Community Acquired Methicillin-Resistant Staphylococcus Aureus Infection. Trials, record NCT00822692. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00822692
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Trial of Septra for Uncomplicated Skin Abscesses in Patients at Risk for Community Acquired Methicillin-Resistant Staphylococcus Aureus Infection
- NCT number
- NCT00822692
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 139 participants, actual
- Lead sponsor
- 59th Medical Wing
- Conditions
- Abscess, Methicillin-Resistant Staphylococcus Aureus Infection
- Interventions
- Trim/ Sulfa DS, placebo
- First posted
- 2009-01-14
- Last updated
- 2015-12-21
- Results first posted
- 2009-09-03
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Recurrence Rates of Abscesses | 30 days after incision and drainage | Number of patient with a new abscess in same or different location as previous lesion |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Recurrence Rates of Abscesses | 30 days after incision and drainage | participants | NUMBER |
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 |
|---|---|---|---|---|---|
| Recurrence Rates of Abscesses | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 4 | participants | ||
| Recurrence Rates of Abscesses | Matched Placebo 2 Pills PO BID x 7 Days | 14 | 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 | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 63 | |
| Overall Study | STARTED | Matched Placebo 2 Pills PO BID x 7 Days | 76 | |
| Overall Study | COMPLETED | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 46 | |
| Overall Study | COMPLETED | Matched Placebo 2 Pills PO BID x 7 Days | 51 | |
| Overall Study | NOT COMPLETED | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 17 | |
| Overall Study | NOT COMPLETED | Matched Placebo 2 Pills PO BID x 7 Days | 25 |
Source ClinicalTrials.gov
Adverse events2
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | treatment failure | Skin and subcutaneous tissue disorders | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 15 | 63 | |
| other | treatment failure | Skin and subcutaneous tissue disorders | Matched Placebo 2 Pills PO BID x 7 Days | 27 | 76 |
Source ClinicalTrials.gov
Adverse event totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | ||
| Total, all-cause mortality | Matched Placebo 2 Pills PO BID x 7 Days | ||
| Total, other adverse events | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 15 | 63 |
| Total, other adverse events | Matched Placebo 2 Pills PO BID x 7 Days | 27 | 76 |
| Total, serious adverse events | Bactrim DS (800/160) Two Tablets PO BID x 7 Days | 0 | 63 |
| Total, serious adverse events | Matched Placebo 2 Pills PO BID x 7 Days | 0 | 76 |
Source ClinicalTrials.gov
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 20346539 | DERIVED |
Source PubMed
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 comparisons2
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Bactrim DS (800/160) Two Tablets PO BID x 7 Days vs Matched Placebo 2 Pills PO BID x 7 Days: Recurrence Rates of Abscesses | Trial comparisons |
| Bactrim DS (800/160) Two Tablets PO BID x 7 Days vs Matched Placebo 2 Pills PO BID x 7 Days: 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/NCT00822692
GET https://conductscience.org/api/trials/v1/NCT00822692/registered