Clinical Trials Directory

Trials / Completed

CompletedNCT02282774

Subtenon Block Combined With General Anesthesia for Vitreoretinal Surgery

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
80 (actual)
Sponsor
King Saud University · Academic / Other
Sex
All
Age
40 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To evaluate the effects of subtenon block (SB) as an adjunct to general anaesthesia on postoperative pain, oculocardiac reflex and postoperative nausea and vomiting for vitreoretinal surgery.

Conditions

Interventions

TypeNameDescription
DRUG2% lidocaine and 0.5% bupivacaineUnder general anesthesia and the operating microscope, a Lieberman lid speculum was placed and the conjunctiva was cleaned with 4% povidone iodine solution. The surgeon then created a fornix-based incision through conjunctiva and tenon's tissue inferonasally midway between the insertions of the medial and inferior rectus muscles, with blunt Wescott scissors to expose the scleral surface before tunneling posteriorly with curved Stevens scissors to create a small channel to the posterior subtenon space. A blunt-tipped subtenon cannula was then inserted into the posterior subtenon space, 4mL of 2% lidocaine and 0.5% bupivacaine (50:50) mixture versus saline was introduced and the drug solution was injected slowly into the subtenon space. After administration of local anesthetic mixture, the eyelid was gently taped down, and no ocular massage was performed
DRUGSham subtenon block

Timeline

Start date
2013-12-01
Primary completion
2014-06-01
First posted
2014-11-04
Last updated
2014-11-04

Locations

1 site across 1 country: Saudi Arabia

Source: ClinicalTrials.gov record NCT02282774. Inclusion in this directory is not an endorsement.