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Management of Thirst, Nursing Care, Postoperative Care

Sponsor
Istanbul Medipol University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04070911
Collaborator
(none)
150
Enrollment
1
Location
3
Arms
31.6
Actual Duration (Months)
4.7
Patients Per Site Per Month

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: WATER
  • Other: ICE APPLICATION
 N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
RANDOMIZED CONTROLLED STUDY GROUPRANDOMIZED CONTROLLED STUDY GROUP
Masking:
Single (Participant)
Primary Purpose:
Supportive Care
Official Title:
The Effect of Oral Water and Ice Popsicle on Management of Thirst in the Immediate Postoperative Period.
Actual Study Start Date :
Nov 24, 2015
Actual Primary Completion Date :
Jul 13, 2018
Actual Study Completion Date :
Jul 13, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: patients in the water group

water group: Patients in the water group were performed oral water after their accession to PACU.

Other: WATER
ORAL WATER
Experimental: patients in the ice group

ice group, Patients in the ice group were performed oral ice popsicle after their accession to PACU.

Other: ICE APPLICATION
ICE APPLICATION
No Intervention: no intervention group

control group, the control group patients have performed rutin treatment and care without any other intervention

Outcome Measures

Primary Outcome Measures

  1. THIRSTY SCALE [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 Outcome Measures

  1. The blood pressure measurements in the first 30 minutes after surgery [first 30 minutes after surgery]

    Blood pressure was obtained from the monitor data of patients who were monitored postoperatively. Blood pressure was measured as "mmHg".

  2. The heart rate measurements in the first 30 minutes after surgery [first 30 minutes after surgery]

    Heart rate was obtained from the monitor data of patients who were monitored postoperatively. heart rate refers to the number of beats per minute.

  3. The respiratory rate measurements in the first 30 minutes after surgery [first 30 minutes after surgery]

    The respiratory rate was obtained from the monitor data of the patients who were monitored postoperatively. respiration rate is the sum of inspiration and expiration per minute.

  4. The body temperature measurements in the first 30 minutes after surgery [first 30 minutes after surgery]

    Body temperature was obtained from the monitor data of patients who were monitored postoperatively. body temperature was recorded with the degree system in degrees Celsius.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

  1. have a surgical operation other than gastrointestinal system surgery,

  2. Surgical fasting duration is at least 8 hours,

  3. According to the American Society of Anesthesiologists (ASA) classification; Class I, II and III;

  4. Having the ability to express the thirst status verbally and experiencing moderate or severe thirst when the thirst status is evaluated by VAS,

  5. The duration of anesthesia is longer than 1 hour and accepted into the PACU after surgery.

Exclusion Criteria:

  1. have a second surgical intervention during hospitalization,

  2. The need of intensive care after surgery,

  3. Having problems in the process of separation from respiratory support after surgical intervention,

  4. A change in the state of consciousness after surgical intervention / acute confusion,

  5. Liquid electrolyte imbalance,

  6. Patients with difficulty in swallowing or restriction of oral fluid intake,

Contacts and Locations

Locations

Site City State Country Postal Code
1 Istanbul Medipol University Kavacık Turkey

Sponsors and Collaborators

  • Istanbul Medipol University Hospital

Investigators

  • Study Director: seher deniz öztekin, Prof.Dr., thesis advisor

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
esra eren, ASSISTANT PROFESSOR, Istanbul Medipol University Hospital
ClinicalTrials.gov Identifier:
NCT04070911
Other Study ID Numbers:
  • 55323
First Posted:
Aug 28, 2019
Last Update Posted:
Aug 28, 2019
Last Verified:
Aug 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by esra eren, ASSISTANT PROFESSOR, Istanbul Medipol University Hospital
Perioperative nursing
Postanesthesia care
Thirst
Water
Ice

Study Results

No Results Posted as of Aug 28, 2019