Trials / Completed
CompletedNCT03729076
Crystalloid Versus Colloid Rapid Co-load for Cesarean Delivery Under Spinal Anesthesia
Crystalloid Versus Colloid Rapid Co-load in Parturients Receiving Prophylactic Phenylephrine Infusion During Cesarean Delivery Under Spinal Anesthesia
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Seoul National University Hospital · Academic / Other
- Sex
- Female
- Age
- 20 Years
- Healthy volunteers
- Not accepted
Summary
The study aims to compare crystalloid co-loading and colloid co-loading in parturients receiving prophylactic phenylephrine infusion during cesarean delivery in terms of the incidence of hypotension.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Crystalloid | Patients will receive the rapid co-loading with plasma solution A (PSA) 10ml/kg, from the initiation of spinal anesthesia, within 10 minutes. |
| OTHER | Colloid | Patients will receive the rapid co-loading with 6% volulyte (HES in acetated electrolyte) 10ml/kg, from the initiation of spinal anesthesia, within 10 minutes. |
Timeline
- Start date
- 2018-11-16
- Primary completion
- 2020-01-08
- Completion
- 2020-01-12
- First posted
- 2018-11-02
- Last updated
- 2020-02-05
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03729076. Inclusion in this directory is not an endorsement.