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This Study Performed to Develop a New Technique for Measuring the Intra Abdominal Pressure

NCT02319213 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2014-12-18

No results posted yet for this study

Summary

The purpose of this study is to evaluate the changes of intraocular pressure due to the increase of intra abdominal pressure.

Conditions

  • Abdominal Compartment Syndrome

Interventions

OTHER

Intraocular pressure measurement with 9 mmHg insufflation

Comparison of intraocular pressure levels at different abdominal pressure

OTHER

Intraocular pressure measurement with 12 mmHg insufflation

Comparison of intraocular pressure levels at different abdominal pressure

OTHER

Intraocular pressure measurement with 15 mmHg insufflation

Comparison of intraocular pressure levels at different abdominal pressure

Sponsors & Collaborators

  • Selcuk University

    lead OTHER

Principal Investigators

  • İlhan Ece · Selcuk Universitesi Tip Fakultesi Genel Cerrahi poliklinigi

Study Design

Allocation
NON_RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2009-01-31
Completion
2009-11-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02319213 on ClinicalTrials.gov