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Comparison of Corneal methods protection during general anesthesia for functional endoscopic sinus surgery

Comparison of Corneal methods protection during general anesthesia for functional endoscopic sinus surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141009019470N114
Enrollment
72
Registered
2021-04-10
Start date
2021-04-18
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

functional endoscopic sinus surgery. Acute sinusitis

Interventions

Intervention 1: Intervention group: In patients of intervention group one, after implantation, the patient's eyelid endotracheal tube will be fixed with standard anti-allergy adhesive. In such a way t

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing sinus surgery by endoscopy ASA I-II

Exclusion criteria

Exclusion criteria: History of any eye disease History of ocular trauma or any congenital or acquired abnormality Any type of eye surgery Pregnancy History of using any type of contact lens in the last week

Design outcomes

Primary

MeasureTime frame
Retinopathy. Timepoint: After transfer to the patient to the recovery room. Method of measurement: fluorescein eye stain test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Shahin Hakimi

Shiraz University of Medical Sciences

masihifarzaneh@yaoo.com+98 71 3647 4270

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026