Ignite Creation Date:
2024-10-26 @ 3:38 PM
Last Modification Date:
2024-10-26 @ 3:38 PM
Study NCT ID:
NCT06571188
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-08-22
Brief Title:
Comparison Of Ultrasound-Guided Continuous Erector Spinae Plane Block Versus Thoracic Epidural Analgesia
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Comparison Of Ultrasound-Guided Continuous Erector Spinae Plane Block Versus Thoracic Epidural Analgesia In Postoperative Analgesia Following Thoracotomy Surgeries A Randomised Trial
Status:
RECRUITING
Status Verified Date:
2024-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
TEAVSESPB
Brief Summary:
There are limited studies comparing these two modalities thoracic epidural and erector spine block for relieving the pain after thoracic surgeries this study aim to investigate this purpose
Detailed Description:
The random sequence will be sealed in consecutively numbered opaque envelopes and kept by the study coordinator Participants will be randomly divided into two groups according to the 11 ratio of ESPB group and TEB group A research coordinator is designated to distribute and preserve randomization result The coordinator will open the envelopes for allocation according to the order of enrolment and prepare the study drug
The participants will be blinded to the allocation Because the needle injection of ESPB and TEB are very close participants themselves could hardly detect the clinical differences Anaesthesiologists who perform the nerve block and take charge of intraoperative management and surgeons are independent individuals Only the random sequence number rather than the specific nerve block type will be recorded in the electronic anaesthesia information management system Researchers who do not take part in the nerve block and intraoperative management are designated to postoperative follow-up Besides trained anaesthesiologist who do not perform the block will be designated to evaluate the clinical features of the block objectively
The participants will be blinded to the allocation Because the needle injection of ESPB and TEB are very close participants themselves could hardly detect the clinical differences Anaesthesiologists who perform the nerve block and take charge of intraoperative management and surgeons are independent individuals Only the random sequence number rather than the specific nerve block type will be recorded in the electronic anaesthesia information management system Researchers who do not take part in the nerve block and intraoperative management are designated to postoperative follow-up Besides trained anaesthesiologist who do not perform the block will be designated to evaluate the clinical features of the block objectively
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None