Clinical Trials Directory

Trials / Completed

CompletedNCT01963299

Clonidine - Ropivacaine in Peribulbar Anesthesia

Prospective Randomised Double-blind Study to Compare Ropivacaine 10mg/mL Alone Versus Ropivacaine 10mg/mL Associated With Clonidine 1µg/kg for Peribulbar Anesthesia in Posterior Eye Surgery

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Centre Hospitalier Universitaire Dijon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a study conducted in 60 patients, randomly assigned to one of two groups of 30: the first will receive ropivacaine alone and the second will receive the association ropivacaine/clonidine. The aim of the study is to prove that the association of Clonidine with Ropivacaine is more effective than ropivacaine alone for locoregional anaesthesia of the eye for retinal surgery. The principal interest of this association of drugs is that it procures faster and longer anaesthesia of the eye with less ropivacaine (therefore fewer injections). This provides greater comfort to the patient during and after the intervention.

Conditions

Interventions

TypeNameDescription
DRUG5 ml Ropivacaine 10% + physiological saline
DRUG5 ml Ropivacaine 10% + Clonidine 1 µg/kg

Timeline

Start date
2013-08-16
Primary completion
2013-10-07
Completion
2013-10-07
First posted
2013-10-16
Last updated
2019-01-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT01963299. Inclusion in this directory is not an endorsement.