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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

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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

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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.

ListOutcomeTime frameDescription
PrimaryRecurrence Rates of Abscesses30 days after incision and drainageNumber of patient with a new abscess in same or different location as previous lesion

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYRecurrence Rates of Abscesses30 days after incision and drainageparticipantsNUMBER

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Recurrence Rates of AbscessesBactrim DS (800/160) Two Tablets PO BID x 7 Days4participants
Recurrence Rates of AbscessesMatched Placebo 2 Pills PO BID x 7 Days14participants

Participant flow6

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDBactrim DS (800/160) Two Tablets PO BID x 7 Days63
Overall StudySTARTEDMatched Placebo 2 Pills PO BID x 7 Days76
Overall StudyCOMPLETEDBactrim DS (800/160) Two Tablets PO BID x 7 Days46
Overall StudyCOMPLETEDMatched Placebo 2 Pills PO BID x 7 Days51
Overall StudyNOT COMPLETEDBactrim DS (800/160) Two Tablets PO BID x 7 Days17
Overall StudyNOT COMPLETEDMatched Placebo 2 Pills PO BID x 7 Days25

Adverse events2

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
othertreatment failureSkin and subcutaneous tissue disordersBactrim DS (800/160) Two Tablets PO BID x 7 Days1563
othertreatment failureSkin and subcutaneous tissue disordersMatched Placebo 2 Pills PO BID x 7 Days2776

Adverse event totals6

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityBactrim DS (800/160) Two Tablets PO BID x 7 Days
Total, all-cause mortalityMatched Placebo 2 Pills PO BID x 7 Days
Total, other adverse eventsBactrim DS (800/160) Two Tablets PO BID x 7 Days1563
Total, other adverse eventsMatched Placebo 2 Pills PO BID x 7 Days2776
Total, serious adverse eventsBactrim DS (800/160) Two Tablets PO BID x 7 Days063
Total, serious adverse eventsMatched Placebo 2 Pills PO BID x 7 Days076

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
20346539DERIVED

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.

ComparisonSource
Bactrim DS (800/160) Two Tablets PO BID x 7 Days vs Matched Placebo 2 Pills PO BID x 7 Days: Recurrence Rates of AbscessesTrial comparisons
Bactrim DS (800/160) Two Tablets PO BID x 7 Days vs Matched Placebo 2 Pills PO BID x 7 Days: serious adverse eventsTrial 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.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

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