Trials / Recruiting
RecruitingNCT05015582
Perioperative Warming Measures in Cesarean Delivery
Randomized Control Trial Assessing Effectiveness of Perioperative Warming Measures in Parturients Undergoing Cesarean Delivery
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- The University of Texas Health Science Center, Houston · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the best method for keeping patients warm during cesarean deliveries and the effect of temperature change on the patient and baby
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Pre op upper body forced air warming (32˚C) | Use of upper body forced air warming at ambient (32˚C) for at least 30 minutes |
| DEVICE | Pre op lower body forced air warming (32˚C) | lower body forced air warming at ambient (32˚C) for at least 30 minutes |
| DEVICE | Pre op fluids (45˚C) | fluids from warmed cabinet set at 45˚C |
| DEVICE | Intra op upper body forced air warming (32˚C) | Use of upper body forced air warming intra-operative at ambient (32˚C) |
| DEVICE | Intra op fluids at room temperature | IV fluids at room temperature |
| DEVICE | Intra op upper body forced air warming at (32˚C) | upper body forced air warming intra-operative at ambient (32˚C) |
| DEVICE | Intra op upper body forced air warming at (42˚C) | upper body forced air warming intra-operative at ambient (42˚C) |
| DEVICE | Intra op lower body forced air warming at (32˚C) | Lower body forced air warming intra-operative at ambient (32˚C) |
| DEVICE | Intra op lower body forced air warming at (42˚C) | Lower body forced air warming intra-operative at ambient (42˚C) |
| DEVICE | Intra op fluid (42˚C) | IV fluids with hotline fluid warmer set at 42˚C |
Timeline
- Start date
- 2021-08-23
- Primary completion
- 2023-08-01
- Completion
- 2023-08-01
- First posted
- 2021-08-20
- Last updated
- 2023-01-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05015582. Inclusion in this directory is not an endorsement.