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Clinical Trials/NCT02149394
NCT02149394
Completed
Not Applicable

Efficacy of Ice Popsicle in the Management of Thirst in the Immediate Postoperative Period: Randomized Clinical Trial

Universidade Estadual de Londrina1 site in 1 country208 target enrollmentAugust 2013
ConditionsThirst

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Thirst
Sponsor
Universidade Estadual de Londrina
Enrollment
208
Locations
1
Primary Endpoint
Change in the intensity of the final thirst assessment with respect to the initial thirst assessment.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to assess the efficacy of ice popsicle compared with water at room temperature in relieving thirst in the immediate postoperative period . The hypothesis of the study is that ice has 20% greater efficacy than water to relieve thirst in the immediate postoperative period.

Detailed Description

There is evidence that ice is effective in relieving thirst in surgical patients, because, by stimulating the oral receptors sensitive to cold, ice decreases the need to ingest large volumes of liquids to satisfy thirst. This way, the risk of bronchoaspiration due to gastric fullness is avoided and discomfort with dry mouth is reduced. Preliminary evidence, therefore, indicates that the use of ice chips have greater efficacy than water at room temperature in relieving thirst. However, there is no scientific evidence from controlled studies with results that can be generalized with respect to a safe volume and adequate frequency of ice administered to reduce thirst in the immediate postoperative period.Considering that the gold standard for the study of a symptom is based on individuals' perceptions and their reports, this study is justified in order to assess the effectiveness of ice compared with water at room temperature in relieving thirst in the immediate postoperative period.

Registry
clinicaltrials.gov
Start Date
August 2013
End Date
December 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marilia Ferrari Conchon

Master of science degree in nursing

Universidade Estadual de Londrina

Eligibility Criteria

Inclusion Criteria

  • aged between 18 and 65 years;
  • undergoing more than eight-hour preoperative fasting;
  • expressing thirst spontaneously or stimulated with intensity greater than or equal to three according to the numeric visual analogue scale;
  • receiving opioids or anticholinergics during surgery;
  • duration of anesthesia exceeding one hour;
  • having been approved in the assessment by the Safety Protocol of Thirst Management;
  • signing the informed consent during the preoperative period.

Exclusion Criteria

  • patients who had intake or swallowing restrictions.

Outcomes

Primary Outcomes

Change in the intensity of the final thirst assessment with respect to the initial thirst assessment.

Time Frame: 1 hour

5 evaluations of thirst intensity every 15 minutes during the first hour postoperatively. Thirst intensity was measured within the range from 1 to 10 in 1.0 intervals as reported by patients when orally required "how thirsty are you now?"according to the visual analogue scale. Zero means not thirsty at all and ten the worst thirst sensation that the patient have ever had.

Secondary Outcomes

  • Reaching the point of satiety over one-hour assessment presented by the experimental and control groups.(1 hour)

Study Sites (1)

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