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The Effect of Forced Air Warming During Cesarean Section on Postoperative Infectious Morbidity

The Effect of Forced Air Warming During Cesarean Section on Postoperative Infectious Morbidity

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00696462
Enrollment
0
Registered
2008-06-12
Start date
2007-03-31
Completion date
2009-04-30
Last updated
2012-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cesarean Section

Keywords

forced-air warming, Bair Hugger, cesarean section, postoperative infection, surgical site infections

Brief summary

The purpose of this study will be to assess whether forced air warming decreases the rate of surgical site infections following cesarean section.

Detailed description

Given the physiologic and experimental evidence regarding temperature regulation; it remains convincing that forced air warming is protective against the development of SSI. We will set out to prospectively study the effect of forced air warming on patients undergoing cesarean section.

Interventions

forced-air warming device

Sponsors

Vanderbilt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adult (≥ 18 years old) female subjects who will undergo cesarean delivery regardless of indication. * Subjects who have signed an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. * Patients scheduled to receive prophylactic antibiotic therapy.

Exclusion criteria

* Patients who are undergoing a true emergent cesarean section that does not allow placement of the warming devices. * Patients undergoing general anesthesia.

Design outcomes

Primary

MeasureTime frame
treatment effects on wound infectionAs is current standard of care post procedure

Secondary

MeasureTime frame
treatment effects on endometritisas is current standard of care post procedure

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026