Clinical Trials Directory

Trials / Completed

CompletedNCT03507426

Retrobulbar Block Versus Ketamine Infusion for Post-enucleation Analgesia

Retrobulbar Block Versus Ketamine Infusion as Adjuvants to General Anesthesia for Post-operative Pain Control After Enucleation

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Nazmy Edward Seif · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study compares the efficacy and safety of two techniques, retrobulbar block versus intra-operative ketamine infusion, for control of post-operative pain occurring in patients undergoing ocular enucleation or evisceration performed under general anesthesia.

Conditions

Interventions

TypeNameDescription
PROCEDURERetrobulbar blockPatients will receive a single retrobulbar injection with 3-4ml of an equal mixture of Lidocaine 2% \& Bupivacaine 0.5% + Hyaluronidase (10 IU/ml), after induction of general anesthesia.
PROCEDUREKetaminePatients will receive a 0.5 mg/kg bolus followed by an infusion of 0.25 mg/kg/h of intravenous Ketamine, after induction of general anesthesia.

Timeline

Start date
2018-04-25
Primary completion
2020-03-31
Completion
2020-03-31
First posted
2018-04-25
Last updated
2020-07-14

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03507426. Inclusion in this directory is not an endorsement.