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

Package of Mentholated Measures for the Relief of Thirst in the Anesthesia Recovery Room: Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02869139
Enrollment
120
Registered
2016-08-16
Start date
2014-04-30
Completion date
2016-01-31
Last updated
2016-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Irritation Lips, Mouth Dryness, Thirst

Keywords

Thirst, Ice, Menthol, Perioperative Nursing., Recovery Room

Brief summary

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

Detailed description

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.

Interventions

OTHERMentholated lip moisturizer and ice popsicle

Mentholated package of measures

OTHERNon-mentholated lip moisturizer and ice popsicle

Non-mentholated package of measures

Sponsors

Universidade Estadual de Londrina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in intensity of thirst, lip hydration, dryness of the mouth and taste the final oral cavity above the original between the experimental and control groups.three times: 0 minutes, 30 minutes and 60 minutes after intervention and evaluationThe evaluation procedures were repeated every 30 minutes for one hour, representing three evaluation moments (M1, M2 and M3).

Secondary

MeasureTime frameDescription
Change in the extent of satiety point over an hour assessment, presented by experimental and control groups, and the number of interventions required in every moment of assessment and intervention for each group.three times: 0 minutes, 30 minutes and 60 minutes after intervention and evaluationThe evaluation procedures were repeated every 30 minutes for one hour, representing three evaluation moments (M1, M2 and M3).

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026