Clinical Trials Directory

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

TypeNameDescription
DRUGGranisetron HydrochloridePatients received Granisetron.
DRUGNo GranisetronPatients 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.