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NCT02939443 Clinical Trial

Prone-position CT for Diagnosing Inguinal Hernia

Hernia, Inguinal Clinical Trial

Official title:
Diagnosis of Inguinal Hernia by Prone- vs. Supine-position Computed Tomography

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02939443
Other study ID # NCH 14-3
Secondary ID
Status Completed
Phase N/A
First received October 14, 2016
Last updated October 18, 2016
Start date April 2014
Est. completion date September 2016

Study information
Verified date October 2016
Source Nagareyama Central Hospital
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

Background: The aim of this study was to investigate the efficacy of prone-position computed tomography (CT) for detecting and classifying inguinal hernia relative to supine-position CT before laparoscopic inguinal hernia repair.

Materials and Methods: Sixty-eight patients who underwent laparoscopic transabdominal preperitoneal repair of inguinal hernia were enrolled in this prospective study. Patients diagnosed with inguinal hernia by physical examination underwent abdominal CT in the supine and prone positions for preoperative assessment. The anatomy of the right and left inguinal regions was confirmed during the surgery and compared with the preoperative CT findings.

Recruitment information / eligibility
Status Completed
Enrollment 68
Est. completion date September 2016
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 89 Years
Eligibility Inclusion Criteria:

- inguinal hernia

Exclusion Criteria:

- emergency surgery for incarcerated hernia

- femoral hernia

- recurrent inguinal hernia after laparoscopic inguinal hernia repair

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Intervention

Radiation:
• supine- and prone-position Computed Tomography

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Nagareyama Central Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary The detection rate of inguinal hernia two years No
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