The Effect of Oral Carbohydrate Inhalation Given to Patients Before Coronary Artery Bypass Graft Operation on Recovery
Investigation of the Effects of Oral Carbohydrate Solution Given to Patients Before Coronary Artery Bypass Graft Surgery on Postoperative Nausea and Vomiting, Feeling of Hunger and Thirst, Physiological Parameters and Recovery
1 other identifier
interventional
120
1 country
1
Brief Summary
The aim of this study was to investigate the effect of oral carbohydrate solution given to patients before coronary artery bypass graft surgery on nausea-vomiting, hunger, thirst, physiologic parameters and recovery. The study will be completed with a total of 120 participants, 40 control, 40 placebo and 40 experimental. As a randomization method, simple randomization method will be used to provide an equal number of samples in three groups and patients will be informed verbally about the study and written informed consent will be obtained from patients who agree. In this study, the effects of oral carbohydrate solution administration on nausea and vomiting, hunger, thirst, physiologic parameters and recovery were evaluated before coronary artery bypass graft surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable surgery
Started Mar 2024
Shorter than P25 for not_applicable surgery
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 8, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 10, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 8, 2024
CompletedFirst Submitted
Initial submission to the registry
December 27, 2024
CompletedFirst Posted
Study publicly available on registry
January 23, 2025
CompletedJanuary 27, 2025
January 1, 2025
2 days
December 27, 2024
January 23, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Patient Information Form
The personal information form used in the data collection process consists of demographic characteristics of the individuals such as age, gender, marital status, occupation, educational status and employment status, as well as health-related conditions of the patients such as chronic diseases and past surgical history.
Up to 24 weeks
Secondary Outcomes (1)
Postoperative Recovery Index (Turkish Version)
Up to 24 weeks
Other Outcomes (3)
Visual Benchmark Scale
Up to 24 weeks
Number and Dosage of Antiemetic Drugs Taken in 24 Hours Postoperatively
Up to 24 weeks
Physiological Parameters and Blood Glucose Monitoring Form
Up to 24 weeks
Study Arms (3)
Oral carbohydrate solution was administered preoperatively
EXPERIMENTALThe experimental group will be given 800 ml of ora carbohydrate solution until midnight before surgery and 400 ml 2 hours before surgery. Patient Information Form will be collected from the patients before surgery. After the surgery, the Visual Comparison Scale, Physiological Parameters and Blood Glucose Monitoring, Form Postoperative Recovery Index (Turkish Version), and the Number and Dosage of Antiemetic Drugs Taken in the Postoperative 24 Hours form will be used.
Flavored Water Applied Before Surgery
PLACEBO COMPARATORThe placebo group will receive 800 ml of flavored water until midnight before surgery and 400 ml 2 hours before surgery. A Patient Information Form will be collected from the patients before surgery. After the surgery, the Visual Comparison Scale, Physiological Parameters and Blood Glucose Monitoring Form, Postoperative Recovery Index (Turkish Version) and the Number and Dosage of Antiemetic Drugs Taken in 24 Hours Postoperatively will be used.
No Preoperative Intervention
NO INTERVENTIONNo intervention will be made to patients who will undergo surgery. Patient Information Form will be collected from the patients before surgery. After the surgery, the Visual Comparison Scale, Physiological Parameters and Blood Glucose Monitoring Form, Postoperative Recovery Index (Turkish Version) and the Number and Dosage of Antiemetic Drugs Taken in 24 Hours Postoperatively will be used.
Interventions
Oral carbohydrate solution will be administered to patients before coronary artery bypass graft operation and its effects on postoperative nausea-vomiting, hunger, thirst, physiological parameters and recovery will be evaluated.
The effects of flavored water given to patients before coronary artery bypass graft operation on postoperative nausea-vomiting, hunger and thirst,
Eligibility Criteria
You may qualify if:
- years of age or older
- Planned coronary artery bypass graft surgery
- Volunteering to participate in the research
You may not qualify if:
- Under 18 years of age
- Not planned coronary artery bypass graft surgery
- Not volunteering to participate in the research
- Cases received as an emergency
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Yasemin Bozkurtlead
Study Sites (1)
Yasemin BOZKURT
Van, Tuşba, 065, Turkey (Türkiye)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Nurse
Study Record Dates
First Submitted
December 27, 2024
First Posted
January 23, 2025
Study Start
March 8, 2024
Primary Completion
March 10, 2024
Study Completion
August 8, 2024
Last Updated
January 27, 2025
Record last verified: 2025-01