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Tap Block and Cesarean Delivery: Efficacy and Consumption of Postoperative Drugs — TAPFANS  

Cesarean Delivery Clinical Trial

Clinical Trial Summary

The purpose of this study is to determine the efficacy of Tap block after cesarean delivery as a component of multimodal analgesia and evaluation of postoperative drugs consumption.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02801968
Study type Interventional
Source S. Anna Hospital
Contact Ilaria Farinelli
Phone +393332082120
Email ilaria.farinelli@unife.it
Status Recruiting
Phase N/A
Start date April 2016
Completion date September 2016
View Details
See also
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