Comparative Study Between Using Combined Propofol Sedation With subTenon's Infusion as Local Anaesthsia to the Eye Versus General Anesthesia for Strabismus Surgery in Adults
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: sedation with subtenon injection of local anesthetic, General Anesthesia (control group).
- Who it may be relevant to
- Registry conditions: Squint Anaesthesia. Basic parameters: 20 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Comparative Study Between Combined Propofol Sedation With subTenon's Infusion Versus General Anesthesia for Strabismus Surgery in Adults
Overview
in this study investigators compare two type of anesthetic technique for squint surgery in adult patient first is general anesthesia versus local anesthesia using subtenon injection of local anesthetic. comparing patient and surgeon satisfaction in each group
Interventions
- Procedure sedation with subtenon injection of local anesthetic
sedation was induced with fentanyl a loading dose of propofol, followed by continuous infusion of propofol, 3-6 mg/k/h to deep sedation. A nasal tube was inserted to prevent airway obstruction. SubTenon's anaesthesia included "standard" solution is a mixture of 2% plain lignocaine, 0.5% plain bupivacaine, and 150 iu hyaluronidase 0.5%. - Procedure General Anesthesia (control group)
General anaesthesia consisted of premedication with midazolam, followed by fentanyl, cis atracrium, propofol, and tracheal intubation
Primary outcome measures
- patient satisfaction in combined propofol/sub-Tenon's anaesthesia in unilateral or bilateral strabismus surgery according to scale from 1 to 10 a one not satisfied and 10 completely satisfied [Time frame: 12 hour after the end of the operation]
Eligibility criteria
Inclusion criteria
- horizontal or cyclovertical strabismus
Exclusion criteria
- previous EOM surgery, retinal detachment, or filter operation. Patients with ocular or neurological problems, mental retardation, deafness, or dementia
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07504354 · Soh-med-25-9----3PD