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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05004532
Other study ID # 19/08/2020 - 223
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2017
Est. completion date July 7, 2020

Study information

Verified date August 2021
Source Erol Olcok Corum Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this study, it was aimed to investigate the analgesic efficacy of the preoperatively applied Transversus Abdominis Plane (TAP) Block in the management of acute appendicitis-related abdominal pain and post-appendectomy pain.


Description:

TAP block creates an analgesic effect by blocking both sensory skin dermotams and viscerosomatic transmission. TAP block with ultrasound was first performed by Hebbard, and the use of USG made the procedure faster and safer. TAP block has been successfully applied for analgesia in procedures such as laparoscopic colocystectomy, inguinal hernia repair, abdominal hysterectomy, prostatectomy and appendectomy. According to the surgical incision to be applied, TAP block is performed from different anatomical regions. It is also applied for pain palliation in intra-abdominal etiologies or rarely for anesthesia in surgical procedures. The analgesic efficacy of TAP block on preoperative abdominal pain and postoperative surgical pain in acute appendicitis was investigated.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date July 7, 2020
Est. primary completion date January 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients over the age of 18 with a diagnosis of acute appendicitis, - with abdominal pain, - tap block applied for perioperative pain management. Exclusion Criteria: - The data of patients who underwent laparoscopic appendectomy - additional surgical procedure other than appendectomy (right hemicolectomy, etc.) - who were diagnosed other than acute appendicitis after the surgical procedure (diverticulitis, tumor, etc.),

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Erol Olcok Corum Training and Research Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Verbal Numerical Pain Scale <4 good pain managment , >4-10 bad pain managment postoperative time 24 hour time
Secondary BMI kg/(m2) preoperative
Secondary weight kg preoperative
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