Trials / Completed
CompletedNCT04046510
Comparaison of 3 Protocols of Ocytocin Administration in C Section
Comparaison of 3 Protocols of Ocytocin Administration in Cesarean Section
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 180 (actual)
- Sponsor
- Mongi Slim Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturients during elective or urgent C section under spinal anesthesia
Detailed description
This study aimed to compare 3 doses of ocytocin in bolus injection and contnious perfusion during C section. these doses determined by: high, intermediate and low doses, were administred to parturients during elective or urgent C section under spinal anesthesia. The aim was to determine the lowest efficient dose to prevent post partum hemorrage and with the lowest incidence of maternal side effects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ocytocin | Administration of lower doses of Ocytocin in bolus and continuous infusion |
Timeline
- Start date
- 2018-09-01
- Primary completion
- 2019-03-31
- Completion
- 2019-07-31
- First posted
- 2019-08-06
- Last updated
- 2019-08-06
Locations
1 site across 1 country: Tunisia
Source: ClinicalTrials.gov record NCT04046510. Inclusion in this directory is not an endorsement.