Actively Recruiting
Smell Memory Method for Patients Before Surgery
Led by Ataturk University · Updated on 2024-05-16
34
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The research is planned as a randomized controlled experimental at Erzurum Atatürk University Health Application and Research Center. The population of the research will include patients who come to the General Surgery Gastroenterology service for laparoscopic cholecystectomy between the specified dates and who meet the criteria for inclusion in the study. In this research, 30 experimental and 30 control group patients will be included in the study in order to perform parametric tests. The data of the research were prepared by the researcher using the literature and similar studies after obtaining ethics committee approval and written permission from the institution where the research would be conducted. "FR.3- Alertness and Sedation Observer Assessment Scale (OAA/S)" and Modified Aldrete Scoring, Awake and Sedation Observer Assessment Scale and "FR.4- MAS and OAA/S Scores Time-Dependent", which includes the Patient's Vital Signs, are used to evaluate the patient's condition. Patients determined by the "Change Table" will be collected by observing them before and after surgery. In the research; In order to more easily overcome the anxiety and confusion that patients who have undergone surgical operations experience during the orientation process while waking up after the case, the patient will be given suggestions regarding the post-anesthesia waking period by testing the menthol smell in the preoperative period. When the patient hears the menthol scent applied during postoperative awakening; It is intended for the patient to remember that his surgery is over, that he needs to wake up and that the medical staff is waiting for him to wake up. In this way, it is thought that the patient's anxiety and complexity during the postoperative awakening period will be eliminated, the patient's vital signs will remain at an optimum level, and a more comfortable reanimation will occur.
CONDITIONS
Official Title
Smell Memory Method for Patients Before Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be over 18 years and under 80 years old
- Must be willing to participate voluntarily
- Must be scheduled for elective laparoscopic cholecystectomy surgery
- Surgery duration should be 1 hour or longer
- Must receive general anesthesia
- Must not have chronic loss of smell
- Must not have communication barriers or hearing, speaking, or perception problems
You will not qualify if you...
- Those who decline to participate
- Patients with problems in smelling
- Patients undergoing emergency surgeries outside the daily surgery list
AI-Screening
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Trial Site Locations
Total: 1 location
1
Mükremin Taşın
Erzurum, Turkey (Türkiye)
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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