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Trials / Completed

CompletedNCT01855529

ROPI Study : Ropivacaine Interest in Postsurgical Pain After Mastectomy

ROPI Study: Evaluation of the Interest of Ropivacaine Streaming in Postoperative Pain After Mastectomy.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Centre Jean Perrin · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

After surgery for breast cancer, the prevalence of chronic pain is estimated between 20 and 68%. They begin after surgery and may persist until more than 6 months. They respond poorly to opioid analgesics impair the quality of life. Among the different postoperative analgesic techniques used, the use of a local anesthetic infiltration continues catheter has advantages including improving the quality of analgesia, with a significant decrease in average of VAS (scale visual Analogue), a decrease in morphine consumption, improving the quality of life of patients. Our study aims to evaluate the effectiveness of a continuous local anesthetic infiltration in the control of postoperative pain after mastectomy.

Conditions

Interventions

TypeNameDescription
DRUGRopivacaine in one arm and placebo (NaCl) in the other arm

Timeline

Start date
2013-04-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2013-05-16
Last updated
2017-09-12

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01855529. Inclusion in this directory is not an endorsement.

ROPI Study : Ropivacaine Interest in Postsurgical Pain After Mastectomy (NCT01855529) · Clinical Trials Directory