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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05311995
Other study ID # 2021/267
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 1, 2021
Est. completion date February 20, 2022

Study information

Verified date March 2022
Source Inonu University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Open appendectomy has been used in the treatment of appendicitis, which is among the most common emergency pathologies worldwide, since the end of the 19th century. In the 20th century, laparoscopic appendectomy came to the fore and the frequency of use increased gradually. Despite the frequency of laparoscopic appendectomy, there is no consensus on the best way to perform each procedural step. One of these steps is the trocar entry areas. In this study, investigator's aim is to compare the trocar entry areas, which are various reports in the literature, and to find the localization with the optimal usage area. 140 patients who underwent laparoscopic appendectomy between 2021-2022 were randomized into four groups and included in the study. Demographic data, peroperative findings, complications, length of stay and post-operative VAS values of the patients were evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 140
Est. completion date February 20, 2022
Est. primary completion date December 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - patients who underwent laparoscopic appendectomy Exclusion Criteria: patients who underwent open surgery and did not want to be involved in the study process

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Only different trocar sites
Only different trocar sites in literature

Locations

Country Name City State
Turkey Ersin Gundogan Kayseri Kocasinan

Sponsors (1)

Lead Sponsor Collaborator
Inonu University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain Intensity measure self reported pain intensity morning. item is scored 0-10 ( 0: no pain- 10: pain as bad as 1 year
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