Overview

Study : LEVOBUPIVACAINE Versus Placebo

Status:
Completed
Trial end date:
2009-05-01
Target enrollment:
0
Participant gender:
Female
Summary
The locoregional anaesthesia is increasingly important in surgical practice, often allowing to simplify per- and post-operative analgesia. caesarian occurs in 20 % of delivery leading to a longer hospitalization because of the pain resulting from the surgery. The Levobupivacaïne (Chirocaïne) administered through catheters placed in the caesarean scars, showed its efficiency in post-operative analgesia. Method : realization of a double blind prospective randomized study, control versus placebo Purpose : to show that the local administration of a unique dose of analgesia reduce the post-operative pain with a little or non-invasive technique
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Centre Hospitalier Universitaire de Saint Etienne
Treatments:
Analgesics
Bupivacaine
Levobupivacaine
Criteria
Inclusion Criteria:

- age > 18 years

- all patients requiring a non-urgent caesarian done according to the Misgav-Ladach
technique

Exclusion Criteria:

- Patients requiring very urgent caesarian

- allergic to levobupivacaïne

- with previous history of alcoholism or drug addiction

- with severe hypotension or an ischemic cardiopathy badly compensated or thyrotoxicoses

- treated with first generation of IMAO (monoamine oxidase inhibitor) or with
anti-arrhytmia drugs with anesthesic activity