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Completed NCT07787416

Comparison of Four Different Methods Used To Relieve Postoperarive Thirst-Related Discomforts

Conditions: Thirst, Dehydration-related Disorders in Postoperative Patients

Sex: All
Ages: 18 Years – 60 Years
Healthy volunteers: No
Phase: NA
Enrollment: 150
Sponsor: Ege University

Location: Afyonkarahisar Health Sciences University Afyonkarahisar

Summary

This study was conducted to compare four different methods applied to relieve thirst-related discomfort after surgery. The study is a prospective, randomized controlled, experimental research conducted at Afyonkarahisar Health Sciences University Health Practice and Research Center General Surgery Clinic. The study took place between November 2022 and April 2023. 150 patients divided into control and intervention groups were included. The study aimed to investigate the effects of four different methods of quenching thirst after surgery on patient outcomes. Data collection tools include Patient Introduction and Follow-up Form, Numerical Verbal Scale (0 10) to measure thirst intensity, Safe Protocol for the Management of Early Post-Operative Thirst, Surgical Period Thirst-Related Discomfort Scale (CDSBRÖ), Perianesthesia Comfort Scale (PCS) and satisfaction level. Numerical Verbal Scale (0-10) was used to determine. The focus of the data study between groups was on postoperative thirst management, patient comfort, and satisfaction with different interventions. The significance level of 0.05 was taken as the criterion in interpreting the results.

Eligibility Criteria

Inclusion Criteria: * Patients between the ages of 18-60 * General anesthesia for at least 1 hour * Absence of open wounds in the mouth and lips * Patients who can express their thirst verbally and score 4 or more on the numerical verbal scale * Patients who voluntarily agreed to participate in our study Exclusion Criteria: * Presence of pain, nausea and vomiting at the time of data collection * Those with DM and Chronic Kidney Failure * Patients who need intensive care after surgery * Those who have absolute oral intake restriction for more than 24 hours before and after surgery

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07787416). StuddyBuddy aggregates publicly available trial information.