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Evaluation of Postoperative Pain in Cases Undergoing Cataract Surgery Under Topical Versus General Anesthesia

Evaluation of Postoperative Pain in Cases Undergoing Cataract Surgery Under Topical Anaesthetic Versus General Anaesthesia

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07287683
Enrollment
50
Registered
2025-12-17
Start date
2025-04-02
Completion date
2026-03-15
Last updated
2025-12-17

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

Conditions

Cataract, General Anesthetic Drug Adverse Reaction, Topical Anaesthesia

Brief summary

Comparison between cataract surgery under local versus general anesthesia regarding postoperative pain, complications and patient satisfaction and need for rescue analgesic intake after surgery The results will be followed up at 24 hrs, 1 week and after one and half month following the surgery.

Detailed description

This prospective randomized controlled study will be carried out on 50 adult patients. Written informed consent will be taken from all prospective cases. The cases will be selected having (ASA1), (ASA II) or (ASA III) physical status in the age range between 20 and 70 years old with cataract eye disease. This study will be performed in Alexandria Main University Hospital, Egypt. Patients will be followed up at 24 hours, 1 week, and 6 weeks after surgery. The following measurements will be recorded 1. Pain will be assessed prior to surgery and after surgery using VAS score at 24 hours, 1 week, and 6 weeks after surgery. 2. Need for analgesic intake after surgery will be assessed for the first 48 hours 3. Complications after surgery as irritation, infection ,and foreign body sensation were assessed 4. Patient satisfaction will be assessed.

Interventions

DRUGTopical Anaesthesia group

This group of patients will only receive topical anaesthesia for Cataract surgery

DRUGGeneral Anaesthesia group

General Anaesthesia will be given to this group undergoing cataract surgery

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

\- Patients with unilateral cataract planned for surgery under topical or general anesthesia

Exclusion criteria

* patients under 20 or over 70 years old Eye infection Patient refusal

Design outcomes

Primary

MeasureTime frameDescription
Post operative painAt 24 hours, one week and 6 weeks following surgeryPostoperative pain will be assessed using the Visual Analogue Scale (VAS), ranging from 0 (no pain) to 10 (worst pain imaginable).

Secondary

MeasureTime frameDescription
1-complications after surgery 2-Patient satisfaction will be measured using the IOWA Satisfaction with Anaesthesia Scale (ISAS), which ranges from 6 (very satisfied) to 3 or less (dissatisfied).Up to 6 weeksComplications including hypotension, nausea and allergic reaction will be assessed after surgery and 24 hours later. satisfaction assessment will evaluate patient safety, pain control, comfort, nausea, interaction with the surgical team, willingness to repeat the anaesthetic, and relaxation during and after surgery. Patient satisfaction will be recorded at one week and six weeks postoperatively.

Countries

Egypt

Outcome results

None listed

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