Peribulbar Block Versus Subtenon's Injection in Redo Vitreoretinal Surgery
- 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
- age between 18 and 80
- Uncooperative patients
- Bleeding disorders
- High axial length (30mm) with previous buckle surgery
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SEQUENTIAL
- Arm && Interventions
Group Intervention Description subtenon's block peribulbar block versus subtenon's block we use the subtenon cannula to inject the local anesthetic mixture peribulbar block peribulbar block versus subtenon's block we use the usual 25G sharp needle to inject the local anesthetic mixture
- Primary Outcome Measures
Name Time Method intraoperative pain during 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
Name Time Method
Trial Locations
- Locations (1)
Research Institute of Ophthalmology
🇪🇬Giza, Egypt