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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: Completed NA study of Infection, sponsored by University of Florida.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
In non-pregnant patients having certain types of surgery with a high risk of infection, prophylactic antibiotics are routinely administered before the surgical procedure begins to ensure that a high level of antibiotic is present in tissue prior to the time that maximum bacterial contamination occurs. However, there has been concern about exposing the fetus in utero to antibiotics. The question to be addressed was whether preoperative antibiotics (as opposed to antibiotics administered after cla
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 |
What the finished NCT00805545 record still lists
NCT00805545 is an interventional study that assigns participants to a tested intervention. The registered 400 participants enrollment target is mid-sized for trials with a published cap, below the 717-participant average among 41 other Infection trials with a reported enrollment target (44% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Infection
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT00805545's enrollment target sits among peer trials
400 12th of 41 higher than 28 of 41 other Infection trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Infection trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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