Clinical trial
The Timing of Prophylactic Antibiotics in Cesarean Section and the Risk of…
NCT00133029 · University of Pennsylvania, Other · Terminated
Key facts
| NCT number | NCT00133029 |
|---|---|
| Title | The Timing of Prophylactic Antibiotics in Cesarean Section and the Risk of Post-operative Febrile Morbidity |
| Lead sponsor | University of Pennsylvania, Other |
| Status | Terminated |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Cesarean Section |
| Intervention type | Drug |
| Interventions | Timing of prophylactic antibiotic administration |
| Start date | Jul 1, 2004 |
| Primary completion | Jul 1, 2006 |
| Completion | Jul 1, 2006 |
| First posted | Aug 22, 2005 |
| Last update posted | Aug 15, 2016 |
| Countries | United States |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: