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Upper Extremity Position and Intraocular Pressure During Spinal Anesthesia: A Randomized Controlled Trial

Upper Extremity Position and Intraocular Pressure During Spinal Anesthesia: A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07424417
Acronym
UEP-IOP
Enrollment
60
Registered
2026-02-20
Start date
2025-11-20
Completion date
2026-02-10
Last updated
2026-05-14

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

Conditions

Intraocular Pressure, Spinal Anesthesia, Surgical Positioning

Keywords

Upper Extremity Position, Intraocular Pressure, Spinal Anesthesia, Surgical Positioning

Brief summary

This prospective randomized controlled trial evaluated the effect of two upper extremity positions on intraocular pressure (IOP) in adult patients undergoing surgery under spinal anesthesia. Participants were randomly assigned to either an arms-at-sides position or a hands-on-chest position. IOP was measured in the right eye using an Icare ic200 rebound tonometer at predefined perioperative time points. Hemodynamic parameters, including mean arterial pressure, heart rate, and oxygen saturation, were also recorded. The primary outcome was the change in IOP from baseline to 30 minutes between the two upper extremity position groups.

Detailed description

Intraocular pressure (IOP) may be influenced by systemic hemodynamics, venous return, episcleral venous pressure, and patient positioning. Although the effects of head and body position on IOP have been investigated, the impact of upper extremity positioning during spinal anesthesia has not been clearly established. This prospective randomized controlled trial was conducted at Elazig Fethi Sekin City Hospital. Adult patients scheduled for elective surgery under spinal anesthesia were enrolled. After written informed consent, participants were randomly assigned to one of two upper extremity positions: arms positioned alongside the body or hands positioned on the chest. IOP was measured in the right eye using an Icare ic200 rebound tonometer. Measurements were obtained at baseline, 15 minutes, and 30 minutes after spinal anesthesia and positioning. Head and neck position was maintained neutral throughout the measurement period. Hemodynamic parameters, including mean arterial pressure, heart rate, and peripheral oxygen saturation, were recorded simultaneously. The primary outcome was the change in IOP from baseline to 30 minutes between the two study groups. Secondary outcomes included IOP change at 15 minutes and perioperative hemodynamic changes.

Interventions

OTHERUpper Extremity Positioning

Participants were assigned to one of two upper extremity positions during spinal anesthesia: arms positioned alongside the body or hands positioned over the chest.

Sponsors

Elazıg Fethi Sekin Sehir Hastanesi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Outcomes Assessor)

Masking description

Due to the nature of the intervention, participants and care providers could not be blinded. However, intraocular pressure measurements were performed by an outcome assessor blinded to group allocation.

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Age between 18 and 80 years * ASA physical status I-III * Scheduled for elective open inguinal hernia repair under spinal anesthesia * Ability to undergo intraocular pressure measurement * Provision of written informed consent

Exclusion criteria

* History of glaucoma or ocular hypertension * Previous ocular surgery or ocular trauma * Active ocular disease or infection * Contraindication to spinal anesthesia * Inability to cooperate with intraocular pressure measurements * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Change in Intraocular Pressure From Baseline to 30 MinutesBaseline and 30 minutes after spinal anesthesia and upper extremity positioningIntraocular pressure was measured in the right eye using an Icare ic200 rebound tonometer. The primary outcome was the change in intraocular pressure from baseline to 30 minutes after spinal anesthesia and upper extremity positioning between the two study groups.

Secondary

MeasureTime frameDescription
Change in Intraocular Pressure From Baseline to 15 MinutesBaseline and 15 minutes after spinal anesthesia and upper extremity positioningIntraocular pressure was measured in the right eye using an Icare ic200 rebound tonometer. This secondary outcome was the change in intraocular pressure from baseline to 15 minutes after spinal anesthesia and upper extremity positioning between the two study groups.
Mean Arterial PressureBaseline, 15 minutes, and 30 minutes after spinal anesthesia and upper extremity positioningMean arterial pressure was recorded simultaneously with intraocular pressure measurements and evaluated between the two study groups.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026