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Clinical Trials/NCT04070911
NCT04070911
Completed
Not Applicable

The Effect of Oral Water and Ice Popsicle on Management of Thirst in the Immediate Postoperative Period.

Istanbul Medipol University Hospital1 site in 1 country150 target enrollmentNovember 24, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Care
Sponsor
Istanbul Medipol University Hospital
Enrollment
150
Locations
1
Primary Endpoint
THIRSTY SCALE
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The study was conducted to determine the effect of oral water and ice popsicle on management of thirst in the immediate postoperative period as experimental.

Detailed Description

Also, it is aimed to evaluate validity and reliability of "Safety Protocol for Management Thirst in the Immediate Postoperative Period Protocol" which is used to take oral water and ice of patients in the immediate postoperative period, as administrative. The study was conducted with 150 patients who are transferred to the postanesthesia care unit (PACU) after their operation and met study criteria. Patients divided into three groups as the study (water group=50, ice group=50) and control (n=50). Patients in the study group were performed oral water/ice popsicle after their accession to PACU. However, the control group patients have performed rutin treatment and care without any other intervention. Physiologic variables and symptoms with thirst were followed in every three group patients at certain times. Data were evaluated by using NCSS (Number Cruncher Statistical System) 2007 program.

Registry
clinicaltrials.gov
Start Date
November 24, 2015
End Date
July 13, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Istanbul Medipol University Hospital
Responsible Party
Principal Investigator
Principal Investigator

esra eren

ASSISTANT PROFESSOR

Istanbul Medipol University Hospital

Eligibility Criteria

Inclusion Criteria

  • have a surgical operation other than gastrointestinal system surgery,
  • Surgical fasting duration is at least 8 hours,
  • According to the American Society of Anesthesiologists (ASA) classification; Class I, II and III;
  • Having the ability to express the thirst status verbally and experiencing moderate or severe thirst when the thirst status is evaluated by VAS,
  • The duration of anesthesia is longer than 1 hour and accepted into the PACU after surgery.

Exclusion Criteria

  • have a second surgical intervention during hospitalization,
  • The need of intensive care after surgery,
  • Having problems in the process of separation from respiratory support after surgical intervention,
  • A change in the state of consciousness after surgical intervention / acute confusion,
  • Liquid electrolyte imbalance,
  • Patients with difficulty in swallowing or restriction of oral fluid intake,

Outcomes

Primary Outcomes

THIRSTY SCALE

Time Frame: first 30 minutes after the surgery

Thirsty and symptoms of thırsty evaluated via vısual analog scale which containing numbers from zero to ten (0-10), "0" is the minumun point, "10" is the maximum point, higher values represent a better situation.

Secondary Outcomes

  • The blood pressure measurements in the first 30 minutes after surgery(first 30 minutes after surgery)
  • The heart rate measurements in the first 30 minutes after surgery(first 30 minutes after surgery)
  • The body temperature measurements in the first 30 minutes after surgery(first 30 minutes after surgery)
  • The respiratory rate measurements in the first 30 minutes after surgery(first 30 minutes after surgery)

Study Sites (1)

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