Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06595875
Status:
COMPLETED
Last Update Posted:
None
First Post:
2024-09-06
Brief Title:
Modified Thoracoabdominal Nerve Block With Perichondrial Approach in Laparoscopic Cholecystectomy Surgery
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Modified Thoracoabdominal Nerve Block With Perichondrial Approach in Laparoscopic Cholecystectomy Surgery A Prospective Randomized Controlled Double-Blind Study
Status:
COMPLETED
Status Verified Date:
2024-10
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:
None
Brief Summary:
Our primary objective is to evaluate the postoperative numerical rating scale scores in patients undergoing laparoscopic cholecystectomy with an m-TAPA block Our secondary objectives are to assess the total amount of rescue analgesia consumed the time to first rescue analgesia patient satisfaction and the occurrence of complications
Detailed Description:
Patients aged 18-65 with American Society of Anesthesiologists physical status I-III undergoing laparoscopic cholecystectomy under general anesthesia were included in the study Patients with contraindications to regional anesthesia impaired consciousness coagulopathy those using anticoagulants those with infection at the procedure site those with allergies to local anesthetics pregnant women and emergency cases were excluded from the study
The primary outcome measures were the numerical rating scale pain scores 0-10 0 no pain 1-3 mild pain 4-6 moderate pain 7-10 severe pain at 0 2 4 8 12 and 24 hours postoperatively The secondary outcome measures included the total amount of rescue analgesic consumed the time to first rescue analgesia the occurrence of complications such as infection hematoma formation and local anesthetic systemic toxicity and patient satisfaction The age gender weight height surgery duration of patients in both groups were recorded A Likert scale 1 not satisfied at all 2 not satisfied 3 neutral 4 satisfied and 5 very satisfied was used to assess patient satisfaction
The primary outcome measures were the numerical rating scale pain scores 0-10 0 no pain 1-3 mild pain 4-6 moderate pain 7-10 severe pain at 0 2 4 8 12 and 24 hours postoperatively The secondary outcome measures included the total amount of rescue analgesic consumed the time to first rescue analgesia the occurrence of complications such as infection hematoma formation and local anesthetic systemic toxicity and patient satisfaction The age gender weight height surgery duration of patients in both groups were recorded A Likert scale 1 not satisfied at all 2 not satisfied 3 neutral 4 satisfied and 5 very satisfied was used to assess patient satisfaction
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