Trials / Completed
CompletedNCT03318536
Effect of Granisetron on Usage of Sympathomimetics During Caesarean Section
Effect of Granisetron on Usage of Sympathomimetics During Caesarean Section - a Retrospective Analysis
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 240 (actual)
- Sponsor
- Johann Wolfgang Goethe University Hospital · Academic / Other
- Sex
- Female
- Age
- —
- Healthy volunteers
- Accepted
Summary
The aim of the present study is to quantify the dose and usage of sympathomimetics used in caesarean section.
Detailed description
Recent metaanalysis showed significantly reduced hypotension and bradycardia in patients undergoing caesarean section in spinal anesthesia when 5-hydroxytryptamine 3 receptor antagonists were used prophylactically. Due to this fact in our clinic the standard procedure was changed. All patients for caesarean section receive Granisetron before spinal anesthesia. The aim of the present study is to evaluate the usage and dose of sympathomimetics during spinal anesthesia. Therefore the investigators will evaluate approximately 120 participants who received granisetron and 120 participants who did not receive 5-hydroxytryptamine 3 receptor antagonists.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Granisetron Hydrochloride | Patients received Granisetron. |
| DRUG | No Granisetron | Patients who did not receive Granisetron. |
Timeline
- Start date
- 2017-10-05
- Primary completion
- 2017-11-01
- Completion
- 2018-02-01
- First posted
- 2017-10-24
- Last updated
- 2018-05-16
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT03318536. Inclusion in this directory is not an endorsement.