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NCT00805545 · ClinicalTrials.gov registry record · NA
Timing of Antibiotic Prophylaxis for Cesarean Deliveries
A NA study of Infection, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 400
- Enrollment target
- 1
- Study location
NCT00805545 is a NA study of Infection that has completed, run by University of Florida. The registered enrollment target is 400 participants, below the 717-participant average among 41 other Infection trials with a reported enrollment target (44% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00805545, a NA study of Infection, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 400 participants
- Enrollment target
- 1
- Study location
Study Summary
The current standard of care to prevent post partum infectious morbidities is to administer antibiotic prophylaxis to all women undergoing a cesarean delivery. The general practice is to administer the antibiotic immediately after the umbilical cord is clamped. This study will compare the incidence of post partum infectious morbidities when the extended spectrum prophylaxis given before the incision time vs. the time of cord clamp.
Conditions Studied
Interventions
- DRUG Antibiotic
Study Locations (1)
Florida
- Shands Hospital - Gainesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2008-11 |
| Est. Completion | 2009-11 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00805545
The ClinicalTrials.gov registry entry for NCT00805545 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 717-participant average among 41 other Infection trials with a reported enrollment target (44% lower). The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Infection appearing as the primary indexed condition, and to 1 intervention - of which Antibiotic is the first listed.
NCT00805545 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT00805545 about?
NCT00805545 is a clinical study titled "Timing of Antibiotic Prophylaxis for Cesarean Deliveries". The current standard of care to prevent post partum infectious morbidities is to administer antibiotic prophylaxis to all women undergoing a cesarean delivery. The general practice is to administer the antibiotic immediately after the umbilical cord is clamped. This study will compare the incidence ...
What is the current status of trial NCT00805545?
This trial is currently completed. It is a NA study. The enrollment target is 400 participants. The study started on 2008-11. Estimated completion is 2009-11.
What conditions does trial NCT00805545 study?
This clinical trial studies the following conditions: Infection.
What interventions are being tested in trial NCT00805545?
The interventions under investigation include: Antibiotic (DRUG).
Who is sponsoring clinical trial NCT00805545?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00805545 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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