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Clinical Trial Summary

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


Clinical Trial Description

In this prospective study, 40 patients undergoing elective surgery were included. Patients were divided into four groups of 10 patients. The control group (Group C) was not subjected to laparoscopic intervention. Laparoscopic surgery was respectively performed with an intra-abdominal pressure of 9, 12 and 15 mmHg in Groups L (low), M (medium), and H (high pressure). Intraocular pressure was measured binocularly in each patient at three different time (before, during and end of surgery) using a contact tonometer. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02319213
Study type Interventional
Source Selcuk University
Contact
Status Completed
Phase N/A
Start date March 2008
Completion date November 2009

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