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Evaluation of Safety and Efficacy of Using Lipsus Device for Oral Wetting

General Surgery Clinical Trial

Official title:
Evaluation of Safety and Efficacy of Using Lipsus Device for Oral Wetting

Clinical Trial Summary

Following waking up from surgery performed under general anesthesia, patients are suffering from discomforting oral dryness, and moreover, they are not allowed drinking for 24 hours. The current management involves the wetting of patient's lips using wet bandage. This action is dependent on the presence of a family member or a nurse, which is not always possible. Many patients describe the oral dryness as a suffering, added to the suffering anyway entailed by surgery.

The investigated Lipsus device is intended for oral wetting, relieving patient's suffering and minimizing the dependence on continuous presence next to patient's bed.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00945022
Study type Interventional
Source IMD Tech Ltd
Contact Hanna Levy, Dr
Phone (972)-4-638-8837
Email hanna@qsitemed.com
Status Not yet recruiting
Phase N/A
Start date October 2011
Completion date April 2012
View Details
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