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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06289543
Other study ID # BVU-ESTELOGLU
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 1, 2023
Est. completion date April 15, 2024

Study information

Verified date February 2024
Source Bezmialem Vakif University
Contact Emine Seyda Teloglu
Phone +905394191544
Email eteloglu@bezmialem.edu.tr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The current preoperative fasting guidelines recommend, applying preoperative carbohydrate solution 2 hours before the operation to minimize prolonged fasting time potential negative effects and improve patient comfort. Fasting after midnight before the operation day is a widespread practice. The major obstacle to preoperative carbohydrate solutions becoming prevalent and extremely long fasting time is the limited product; which is proven safe and efficient, and unavailable in several countries. In this study, our objective is to analyze the gastric volume, preoperative anxiety, stress response, postoperative insulin resistance, and postoperative nausea and vomiting by utilizing a low osmolality oral carbohydrate solution prepared with ginger and melissa.


Description:

The current preoperative fasting guidelines recommend, applying preoperative carbohydrate solution 2 hours before the operation to minimize prolonged fasting time potential negative effects and improve patient comfort. Fasting after midnight before the operation day is a widespread practice. The major obstacle to preoperative carbohydrate solutions becoming prevalent and extremely long fasting time is the limited product; which is proven safe and efficient, and unavailable in several countries. In this study, our objective is to analyze the gastric volume, preoperative anxiety, stress response, postoperative insulin resistance, and postoperative nausea and vomiting by utilizing a low osmolality oral carbohydrate solution prepared with ginger and melissa. 109 patients who underwent elective laparoscopic cholecystectomy, aged 18-65 years, and ASA physical state 1-2 were included in the study. The patients were divided into 3 groups: Group A, who would not eat anything 6-8 hours before the operation, Group S, who drank 400 ml of water 2 hours before the operation, and Group K, which drank 400 ml preoperative oral carbohydrate solution (PreOKH) 2 hours before the operation. Before induction of anesthesia (T1), patients' antral gastric cross-sectional area (GKA) and gastric volume (GV) were evaluated by gastric ultrasound. The preoperative anxiety level of the patients was determined by the State-Trait Anxiety Inventory (STAl) before the operation (T1), and the symptoms affecting the preoperative patient comfort parameters (thirst, hunger, dry mouth, fatigue) were measured 2 hours before the operation (T0) and before the induction (T1) evaluated with the visual analog scale (VAS). Postoperative nausea and vomiting (PONV) and postoperative pain levels were recorded. Blood glucose, insulin, and cortisol levels of the patients were measured 2 hours before the operation (T0), before induction (T1), and postoperative 2nd hour (T3)


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date April 15, 2024
Est. primary completion date April 1, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Between the ages of 18-65 - Elective laparoscopic cholecystectomy planned under general anesthesia - American Society of Anesthesiologists (ASA) class I-II physical condition Exclusion Criteria: Patients with gastroesophageal reflux and gastrointestinal motility disorders diabetes mellitus Mental retardation, previous neurological disease symptoms (syncope, dementia, Alzheimer, etc.) Chronic alcoholism Difficult Intubation Patients with ASA physical status classes =III Patients with a body mass index of 35 and above History of Meniere and motion sickness Presence of previous history of postoperative nausea and vomiting Smoking

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Preoperative carbohydrate solution
water and solution will be given to patients to drink 2 hours before the operation

Locations

Country Name City State
Turkey Bezmialem University Istanbul Fatih

Sponsors (1)

Lead Sponsor Collaborator
Bezmialem Vakif University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gastric volume Assessment of gastric volume by ultrasound prior to anesthesia induction
Secondary preoperative anxiety preoperative anxiety will be assessed with the State-Trait Anxiety Inventory before coming to the operating room, Scored between 20 and 80 points. A high score indicates high anxiety
Secondary postoperative nausea and vomiting postoperative nausea and vomiting scores of the patients will be evaluated up to postoperative 24 hours, numeric rank score is scored between 0 and 3 points
Secondary thirst, hunger, fatigue, dry mouth thirst, hunger, fatigue, dry mouth will be evaluated with visual analog scale before drink (2 hous before surgery), prior to anesthesia induction, visual analog scale is scored between 0 and 10
Secondary Postoperative Pain Score Postoperative Pain Score will be evaluated with visual analog scale up to postoperative 24 hours, visual analog scale is scored between 0 and 10
Secondary postoperative insulin resistance Blood glucose mg/dL, Insulin milli-International unit/L, Cortisol µg/dL glucose, insulin and cortisol will be measured 2 hours before surgery(before drink), before induction and 2 hours postoperatively
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