Clinical Trials Directory

Trials / Completed

CompletedNCT01458431

Levobupivacaine to the Surgical Wound Following Cesarean

Efficacy of Continuous Infusion of Levobupivacaine to the Surgical Wound Following Cesarean

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
70 (actual)
Sponsor
Manuel Ángel Gómez-Ríos · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The postoperative period following cesarean is associated with moderate to severe pain that requires a considerable amount of analgesics that carry with them side-effects such as nausea, vomiting, fatigue and immobilization. Several studies have tried, with variable results, to find a more effective analgesia alternative such as infusion of local anesthetics through a catheter in the surgical wound sinus, a practice that has currently been widely used in clinical practice. Despite existing references on its use in the postoperative period following cesareans there continues to be a lack of information on other aspects. The investigators study hypothesis is that the use of levobupivacaine in the surgical wound will reduce the surface of hyperalgesia compared to the control group.

Conditions

Interventions

TypeNameDescription
DRUGLevobupivacainecontinuous levobupivacaine subfascial infusion
DRUGNaClcontinuous NaCl subfascial infusion

Timeline

Start date
2011-10-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2011-10-24
Last updated
2014-12-23

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT01458431. Inclusion in this directory is not an endorsement.