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Comparison of alkalinised and non- alkalinised peribulbar anaesthesia in attaining akinesia among patients undergoing cataract surgery: a randomised controlled trial

Comparison of alkalinised and non- alkalinised peribulbar anaesthesia in attaining akinesia among patients undergoing cataract surgery: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202212745220111
Enrollment
224
Registered
2022-12-12
Start date
2022-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Eye Diseases Anaesthesia

Interventions

alkalinised group
non alkalinised group

Sponsors

Gbemisola Borisade
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults aged 40 years and above with operable cataract booked for elective cataract surgery under local anaesthesia

Exclusion criteria

Exclusion criteria: patients with an only eye allergy to any of the medications to be used axial length greater than 26mm patients with neurological manifestations patients unable to follow instructions patients with cognitive impairment active cardiac or respiratory disease poor communication ability such as deafness patient with excessive tremors and agitations

Design outcomes

Primary

MeasureTime frame
injection pain perception, onset and duration of akinesia and anaesthesia are primary outcome measures while secondary outcome measures will be complications of anaesthesia and onset of post operative pain

Secondary

MeasureTime frame
complications from anaesthesia and onset of post operative pain

Countries

Nigeria

Contacts

Public ContactOpeyemi Borisade

Accountant

borisadeope@yahoo.com+2348063354533

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026