Ignite Creation Date:
2024-05-11 @ 8:31 AM
Last Modification Date:
2024-10-26 @ 3:29 PM
Study NCT ID:
NCT06407037
Status:
RECRUITING
Last Update Posted:
2024-05-17
First Post:
2024-05-06
Brief Title:
Comparison of Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block
Sponsor:
Diskapi Yildirim Beyazit Education and Research Hospital
Organization:
Diskapi Yildirim Beyazit Education and Research Hospital
Study Overview
Official Title:
Comparison of the Effects of Ultrasound-Guided Erector Spinae Plane Block and Serratus Posterior Superior Intercostal Plane Block on Postoperative Acute Pain in Patients Undergoing Breast Surgery
Status:
RECRUITING
Status Verified Date:
2024-05
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:
Breast cancer is the most common malignancy in women Modified radical mastectomy a surgical procedure in the treatment of breast cancer is one of the standard treatments Postoperative pain can seriously reduce the quality of life in patients and inadequately treated acute pain can trigger chronic pain syndrome Therefore thoracic paravertebral block and thoracic epidural block are effective in postoperative analgesia However the use of these blocks is limited due to complications In recent years less invasive blocks such as pectoral nerve block PECS I-II Serratus anterior plane block SAPB Erector spinae plane block ESPB and Serratus Posterior Superior intercostal Plane Block SPSİPB have been applied In this study it was aimed to compare the analgesic effectiveness of ESPB and SPSİPB applications in patients undergoing breast surgery
Detailed Description:
Postoperative pain will be assessed during resting and coughing with a Numeric Pain Scale NRS and nausea and vomiting with a Postoperative Nausea Vomiting Score at the postoperative 1 4 8 12 and 24 hours The amount of tramadol consumed in the postoperative period will be recorded Patient satisfaction will be assessed with the Likert scale at postoperative 24 hours
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