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Dexmedetomidine in Topical Versus Peribulbar Anesthesia for Cataract Surgery

Dexmedetomidine as an Additive to Topical Versus Peribulbar Anesthesia for Cataract Surgery

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05692167
Enrollment
94
Registered
2023-01-20
Start date
2023-07-15
Completion date
2023-10-15
Last updated
2023-09-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Cataract Surgery, Dexmedetomidine, Peribulbar

Brief summary

The aim of this study is to compare efficacy of dexmedetomidine as an additive to topical versus peribulbar anesthesia for cataract surgery

Detailed description

Ocular surgery may be performed under topical, regional, or general anesthesia. The first recorded use of regional anesthesia for surgery was the instillation of cocaine into the conjunctival sac in 1884 by an Austrian ophthalmologist. Davis and Mandel in 1986 described the peribulbar block, peribulbar block has delayed onset and need a higher volume of local anesthetic (LA) than a retrobulbar block. But the peribulbar block is away from intra-conal space and so produce fewer complication. Dexmedetomidine is used as adjuvant to LA drugs in peripheral nerve block, brachial plexus block and intrathecal anesthesia with satisfactory results. A more recent study using dexmedetomidine (50 μg) with the peribulbar block before cataract surgery demonstrated an IOP decrease similar to IV dexmedetomidine administration and greater than a peribulbar block without dexmedetomidine.

Interventions

DRUGTopical dexmedetomidine

Patients will receive mixture of one milliliter of dexmedetomidine-HCl and local anesthetic

DRUGReginal dexmedetomidine

Patients will receive mixture of bupivacaine 0.5% (4.5 ml) + lidocaine 2% (4.5 ml) + dexmedetomidine 50 μg (1 ml) in peribulbar block

Sponsors

Kafrelsheikh University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists (ASA) physical status classification I or II who scheduled for eye surgery

Exclusion criteria

* Patients who are younger than 18 years * The usual contraindications for regional anesthesia such as patients refusing LA * Clotting abnormalities * Impaired mental status * Allergy to any of the study medications * patients had the severe cardiac disease * chronic obstructive lung disease and a history of sleep apnea * contraindications to the use of dexmedetomidine * history or significant cardiovascular disease risk factors * significant coronary artery disease or any known genetic predisposition * history of any kind of drug allergy * drug abuse * psychological or other emotional problems * special diet or lifestyle * clinically significant abnormal findings in physical examination * electrocardiographic (ECG) or laboratory screening * known systemic disease requiring the use of anticoagulants.

Design outcomes

Primary

MeasureTime frameDescription
Inadvertent eye movement2 hours postoperativelyAsses intra-ocular pressure (IOP) before injection of baseline and after a complete akinesia of the globe before surgical incision.

Secondary

MeasureTime frameDescription
Anesthesia-related complications2 hours postoperativelyThe patients will be asked whether the cataract surgery was more or less painful than having the needle used for intravenous infusions inserted into the back of the hand.
Sedation level2 hours postoperativelyNumeric Rating Scale will be applied to grade the pain where 0 = no pain and 10 = extreme pain.
pain during and after the surgery2 hours postoperativelyImmediately after surgery, patients will be asked to grade the pain felt during the operation, including the pain felt after delivery of topical or peribulbar anaesthesia.
Need for additional anesthesia during surgery and surgeonDuring surgeryThe dose of additional needed anesthesia (fentanyl 0.5 µg/kg) during surgery will be recorded
Intraoperative difficulties2 hours postoperativelyThe surgeon will also be requested to grade any difficulties encountered during surgery immediately after the operation, using a 4-point scale, where 1 = no difficulty and 4 = extremely difficult

Countries

Egypt

Contacts

Primary ContactMohammed F Algyar, MD
mohammad.algaiar@med.kfs.edu.eg00201111645345

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026