Viewing Study NCT05790317



Ignite Creation Date: 2024-05-06 @ 6:49 PM
Last Modification Date: 2024-10-26 @ 2:55 PM
Study NCT ID: NCT05790317
Status: COMPLETED
Last Update Posted: 2023-03-30
First Post: 2022-12-18

Brief Title: Comparison of the Effect of Traditional Method and Eras Protocol in Obesity Surgery
Sponsor: Bahçeşehir University
Organization: Bahçeşehir University

Study Overview

Official Title: Comparıson Of The Effects Of The Eras Protocol Applıcatıon And The Effects Of The Tradıtıonal Method On The In Obesıty Surgery
Status: COMPLETED
Status Verified Date: 2023-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This study was conducted to compare the effectiveness of care based on the Accelerated Recovery After Surgery ERAS Protocol and the traditional method in bariatric surgery and demonstrate the difference the two methods based on evidence
Detailed Description: The population of the study consisted of 700 patients over the age of 18 who underwent bariatric surgery in the Obesity Surgery Clinic of a private hospital in 2022 The sample of the study included 128 patients who were willing to undergo bariatric surgery between April 15-July 31 2022 were in compliance with the research criteria and were voluntarily over the age of 18 64 in the control and 64 in the experimental group 128 patients in the sample were assigned to 2 groups using a computer program that generates random numbers For the purpose of the research groups were coded as groups A and B and two different surgical preparations and surgical procedures were applied to the patients in the group The effects of two different surgical method preparations and the surgical process on the patients recovery were compared In the study the data were collected with the personal introduction form introducing the characteristics of the patients the Rhodes Nausea-Vomiting and Regurgitation Index WPI the Mcgill Pain Scale and the Postoperative Evaluation Form created within the scope of the ERAS Accelerated Care Protocol Permission was obtained for the scales and the content validity calculation of the Postoperative Evaluation Form was made in line with the evaluations of the field experts consisting of physicians and nurses experienced in the ERAS Rapid Care Protocol The data were analyzed in SPSS Package Program While calculating frequency percentage and standard deviation in the evaluation of the data comparisons between groups were made with the independent sample t-test and p 005 was taken as the significance value of the findings

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None