NCT02061644

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Mar 2014

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 10, 2014

Completed
3 days until next milestone

First Posted

Study publicly available on registry

February 13, 2014

Completed
16 days until next milestone

Study Start

First participant enrolled

March 1, 2014

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2014

Completed
Last Updated

April 7, 2014

Status Verified

April 1, 2014

Enrollment Period

1 month

First QC Date

February 10, 2014

Last Update Submit

April 4, 2014

Conditions

Intraocular Pressure

Outcome Measures

Primary Outcomes (1)

  • Number of the patients with changed intraocular pressure

    One month

Study Arms (1)

Spinal

EXPERIMENTAL

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

Spinal anesthesiaOTHER

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

Spinal

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Adiyaman University Research Hospital

Adıyaman, 02000, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Anesthesia, Spinal

Intervention Hierarchy (Ancestors)

Anesthesia, ConductionAnesthesiaAnesthesia and Analgesia

Study Officials

  • Ruslan Abdullayev, Dr

    Adiyaman University Research Hospital, Department of Anesthesiology and Reanimation, Adiyaman City, Turkey.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
DIAGNOSTIC
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Ruslan Abdullayev

Study Record Dates

First Submitted

February 10, 2014

First Posted

February 13, 2014

Study Start

March 1, 2014

Primary Completion

April 1, 2014

Study Completion

April 1, 2014

Last Updated

April 7, 2014

Record last verified: 2014-04

Locations

TU(1)