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CompletedNCT02061644Updated Apr 7, 2014

Spinal Anesthesia - Intraocular Pressure

An interventional study of Spinal anesthesia in Intraocular Pressure, sponsored by Adiyaman University Research Hospital. Completed at 1 site in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2014-04-07.

Sponsored by Adiyaman University Research Hospital · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
18 Years to 65 Years
Sex
All
01

Study summary

We aim to investigate the effect of spinal anesthesia on intraocular pressure.

Read the detailed description

Spinal anesthesia provides adequate anesthetic conditions for many operations. These operations include orthopedic, urological, gynecological and many general surgery operations. Although few, side effects of the procedure and its effects on body are well known. However, there is inadequate knowledge about the effects of spinal anesthesia on pressure changes in the eyes. These pressure changes in eyes can result in some detriments. Elevated pressures in the eyes can result in disease known as glaucoma, that makes hazard to eyes. Decreased eye pressures can also result in some eye detriments.

We aimed to investigate the effects of spinal anesthesia procedure on eye (intraocular) pressure changes.

02

Conditions studied

  • Intraocular Pressure
03

In context

Lead sponsor

Adiyaman University Research Hospital is the lead sponsor of 48 studies on the registry; 9 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients having general surgery operations under umbilicus
  • patients of American Society of Anesthesiologists (ASA) status I-II

Exclusion criteria

Exclusion Criteria:

  • patients denying spinal anesthesia
  • contraindications for spinal anesthesia
  • eye diseases
  • hypertension
  • ASA status III or more
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
40 participants (actual)

Study arms

  • Experimental
    Spinal

    Spinal anesthesia for surgical procedure will be applied to the patients. Intraocular pressures will be measured before and after the procedure.

    Other: Spinal anesthesia

Interventions

  • OtherSpinal anesthesia

    Routine spinal anesthesia procedure will be made to the patients for surgical anesthesia.

06

What researchers measure

Primary outcomes

  1. Number of the patients with changed intraocular pressure

    Time frame: One month

07

Study locations

1 site
  • Adiyaman University Research Hospital
    Adiyaman, 02000, Turkey
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 7, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02061644
Lead sponsor
Adiyaman University Research Hospital
Responsible party
Ruslan Abdullayev (Dr. Ruslan Abdullayev, Adiyaman University Research Hospital) — Principal investigator
First posted
Feb 13, 2014
Start date
Mar 2014
Primary completion
Apr 2014
Completion
Apr 2014
Last update
Apr 7, 2014

Study contacts

Ruslan Abdullayev, Dr
principal investigator · Adiyaman University Research Hospital, Department of Anesthesiology and Reanimation, Adiyaman City, Turkey.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2014. You cannot join it, but the record below documents what was studied.

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