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Peribulbar Block Versus Subtenon's Injection in Redo Vitreoretinal Surgery

Not Applicable
Recruiting
Conditions
Analgesia
Interventions
Procedure: peribulbar block versus subtenon's block
Registration Number
NCT04978415
Lead Sponsor
Abeer Samir Salem
Brief Summary

To compare the efficacy and efficiency of peribulbar block versus sub-Tenon's capsule injection of local anesthetic in redo vitreoretinal surgery

Detailed Description

Sixty patients undergoing vitreoretinal surgery were randomized to receive either peribulbar or sub-Tenon's capsule injection of 8 ml of a 20:80 mixture of 2% lidocaine and 0.5% bupivacaine with 60 IU hyalouronic acid.

The primary outcome measured was intraoperative eye pain, which was rated by patients in both groups using an 11-point (0-10) numerical visual analogue scale immediately after.

The surgeons indicated whether they perceived patient discomfort during 4 different stages of the operation: opening of the conjunctiva, vitrectomy (if performed), placement of scleral buckle (if performed) or using the laser probe, and closing of the conjunctiva.

The need for supplemental local anesthesia, and use of IV sedation for additional pain control intraoperatively were compared between the two groups.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • age between 18 and 80
Exclusion Criteria
  • Uncooperative patients
  • Bleeding disorders
  • High axial length (30mm) with previous buckle surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
subtenon's blockperibulbar block versus subtenon's blockwe use the subtenon cannula to inject the local anesthetic mixture
peribulbar blockperibulbar block versus subtenon's blockwe use the usual 25G sharp needle to inject the local anesthetic mixture
Primary Outcome Measures
NameTimeMethod
intraoperative painduring whole surgery duration (around 2 hours)

11 point verbal rating score from 0 to 10 where 0 is no pain and 10 is intolerable pain patient will be asked immediately after surgery about pain the need for intraoperative sedation will be recorded

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Research Institute of Ophthalmology

🇪🇬

Giza, Egypt

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