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Comparing Conscious Sedation to Retrobulbar Block Anesthetics During Trans-scleral Diode Laser

NCT03646500 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2018-08-28

No results posted yet for this study

Summary

This is a non-inferiority trial with a prospective randomized controlled design assessing patient satisfaction and complications associated with both retrobulbar block anesthetics (current gold standard) and conscious IV sedation alone (alternative choice of anesthesia) for trans-scleral diode laser (TSD). Patient satisfaction and complications will be measured using standardized patient surveys.

Conditions

Interventions

PROCEDURE

Retrobulbar Block

Anesthetic nerve block administered in the retrobulbar space prior to transcleral diode procedure

PROCEDURE

Remifentanil

Remifentanil administered as intravenous infusion prior to transcleral diode procedure

Sponsors & Collaborators

  • Queen's University

    lead OTHER

Principal Investigators

  • Delan Jinapriya, MD · Queen's University - School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-07-31
Primary Completion
2017-08-31
Completion
2017-10-31

Countries

  • Canada

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03646500 on ClinicalTrials.gov