Package of Mentholated Measures for the Relief of Thirst in the Anesthesia Recovery Room

NCT ID: NCT02869139

Last Updated: 2016-08-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-04-30

Study Completion Date

2016-01-31

Brief Summary

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Package of mentholated measures for the relief of thirst in the anesthesia recovery room: Randomized clinical trial

Detailed Description

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Perioperative thirst is intense and has a high incidence. There is evidence that strategies using cold and menthol could be viable alternatives to reduce thirst and the discomforts arising from it. For that reason, this study evaluated the efficacy of a mentholated package of measures (lip moisturizer and ice popsicle) compared to a non-mentholated package of measures in alleviating thirst in the anesthesia recovery room.

Conditions

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Thirst Mouth Dryness Irritation Lips

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Package of mentholated measures

Package of mentholated measures (mentholated Ice Popsicle and lip moisturizing) Group.

Group Type EXPERIMENTAL

Mentholated lip moisturizer and ice popsicle

Intervention Type OTHER

Mentholated package of measures

Package of non-mentholated measures

Package of non-mentholated measures (mentholated Ice Popsicle and lip moisturizing) Group.

Group Type ACTIVE_COMPARATOR

Non-mentholated lip moisturizer and ice popsicle

Intervention Type OTHER

Non-mentholated package of measures

Interventions

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Mentholated lip moisturizer and ice popsicle

Mentholated package of measures

Intervention Type OTHER

Non-mentholated lip moisturizer and ice popsicle

Non-mentholated package of measures

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Possess aged between eighteen and sixty-five years
* To be fasting for more than four hours
* Verbalizing headquarters spontaneously or after questioning, with greater than or equal to three intensity in numerical verbal scale
* Receive opioids or anticholinergic during surgery duration of greater than one hour anesthesia
* Being in anesthetic recovery in anesthesia recovery room
* Have been approved in the evaluation Headquarter Insurance Management Protocol which was applied to both groups
* Accept participate and sign the consent form Clarified

Exclusion Criteria

* Being allergic to menthol
* Have continuity of injury in the oral mucosa
* Having suspended the anesthetic-surgical procedure after acceptance of participation
* Receive High operating room directly to another healthcare sector than the anesthetic recovery room, and intensive care unit or hospital unit
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Universidade Estadual de Londrina

OTHER

Sponsor Role lead

Responsible Party

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Viviane Moreira Serato

Principal Investigator, Master's degree in Nursing

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Viviane Serato

Role: PRINCIPAL_INVESTIGATOR

Universidade Estadual de Londrina

Locations

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Viviane Moreira Serato

Londrina, ParanĂ¡, Brazil

Site Status

Countries

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Brazil

Other Identifiers

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GPS Menthol

Identifier Type: -

Identifier Source: org_study_id

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