NCT Number: NCT02939443
Prone-position CT for Diagnosing Inguinal Hernia
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.
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Notify MeKey information
Conditions
Age range
20 year–89 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- inguinal hernia
Exclusion criteria
- emergency surgery for incarcerated hernia
- femoral hernia
- recurrent inguinal hernia after laparoscopic inguinal hernia repair
Treatment and study plan
Primary outcomes
-
The detection rate of inguinal hernia
Time frame: two years
Sponsors and collaborators
Lead sponsor
Nagareyama Central Hospital
Other
Registry information
Official study title
Diagnosis of Inguinal Hernia by Prone- vs. Supine-position Computed Tomography
Important dates
- Study start
- 2014
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Oct 20, 2016
- Registry last updated
- Oct 20, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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