Ignite Creation Date:
2024-07-17 @ 12:08 PM
Last Modification Date:
2024-10-26 @ 3:32 PM
Study NCT ID:
NCT06461832
Status:
RECRUITING
Last Update Posted:
2024-07-08
First Post:
2024-06-11
Brief Title:
The Impact of the Anaesthetic Technique Employed on the Quality of Recovery in Patients Undergoing Hysterectomy Surgery
Sponsor:
Samsun University
Organization:
Samsun University
Study Overview
Official Title:
Comparison of Combined Spinal-Epidural Anesthesia and General Anesthesia With Epidural Catheter for Elective Hysterectomy Anesthetic and Analgesic Outcomes Patient and Surgeon Satisfaction A Prospective Observational Study
Status:
RECRUITING
Status Verified Date:
2024-07
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:
The objective of this study is to evaluate the results of different anesthesia methods general anesthesia with epidural catheter application and spinal anesthesia with epidural catheter application applied in elective hysterectomy surgeries performed in our hospital The aim is to compare the advantages of both methods
Detailed Description:
The study was designed as a prospective observational study The researchers participating in the study were not involved in administering any medications to the patients A review of the patient records will result in the creation of two differentiated groups according to the anesthesia method administered Group 1 will include patients who underwent general anesthesia with an epidural catheter while Group 2 will include patients who underwent spinal anesthesia with an epidural catheter The quality of recovery score will be evaluated using a 15-question scale both preoperatively and postoperatively The researchers will evaluate quality of recovery using the 15-item Quality of Recovery scale QoR-15
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