NCT06788951

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable surgery

Timeline
Completed

Started Mar 2024

Shorter than P25 for not_applicable surgery

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2024

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 8, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

December 27, 2024

Completed
27 days until next milestone

First Posted

Study publicly available on registry

January 23, 2025

Completed
Last Updated

January 27, 2025

Status Verified

January 1, 2025

Enrollment Period

2 days

First QC Date

December 27, 2024

Last Update Submit

January 23, 2025

Conditions

Keywords

SurgeryERASNursingCardiovascular

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

EXPERIMENTAL

The 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.

Dietary Supplement: administration of oral carbohydrate solution to patients before coronary artery bypass graft surgery

Flavored Water Applied Before Surgery

PLACEBO COMPARATOR

The 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.

Other: giving flavored water to patients before coronary artery bypass graft surgery

No Preoperative Intervention

NO INTERVENTION

No 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.

Oral carbohydrate solution was administered preoperatively

The effects of flavored water given to patients before coronary artery bypass graft operation on postoperative nausea-vomiting, hunger and thirst,

Flavored Water Applied Before Surgery

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Yasemin BOZKURT

Van, Tuşba, 065, Turkey (Türkiye)

Location

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

Locations