- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03703752
CT and Clinical Features of Internal Hernia
October 11, 2018 updated by: Lei Dou, Tongji Hospital
CT Images and Clinical Relevance of Internal Hernia
Researchers retrospectively reviewed patients with internal hernia that confirmed by surgical exploration between Feb. 2012 and Feb. 2018.
and analysis the Medical records and MDCT images to investigate the clinical and radiological features of internal hernia.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
51 Patients with definite diagnosis of IH during surgical exploration from Feb. 2012 to Feb. 2018 in our hospital were included in this research.
Medical records including MDCT images and intra-operative findings were collected retrospectively.
The CT features of different subgroups were also evaluated.
Study Type
Observational
Enrollment (Actual)
51
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Hubei
-
Wuhan, Hubei, China, 430030
- Tongji Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All Patients with definite diagnosis of IH during surgical exploration from Feb. 2012 to Feb. 2018 in our hospital were included in this research
Description
Inclusion Criteria:
- IH confirmed by surgical exploration
Exclusion Criteria:
- diaphragmatic hernia and traumatic IH
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Adhesive IH
Adhesive IH can further be divided into primary or secondary groups according to the history of abdominal and(or) pelvic surgery
|
This is a diagnostic radiological test to diagnose the IH and evaluate the clinical condition of IH
|
|
non-adhesive IH
Non-adhesive IH means the IH resulting from the abnormality of peritoneal structure.
|
This is a diagnostic radiological test to diagnose the IH and evaluate the clinical condition of IH
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
CT features
Time Frame: 2 weeks
|
MDCT features of IH were assessed for the following findings: (1) Demonstration of bowels dislocation in IH: dislocated cluster of the intestinal segments; crowding or convergence of mesenteric vessels; (2) Demonstration of obstruction or ischemia: bowel wall thickening or abnormal enhancement; dilated bowels with abnormal free fluid; twisted bowels with swirl sign of vessels.
(3) Demonstration of specific signs: hernial orifice and closed-loop of intestine; fat notch sign.
|
2 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 20, 2018
Primary Completion (Actual)
June 20, 2018
Study Completion (Actual)
June 20, 2018
Study Registration Dates
First Submitted
October 9, 2018
First Submitted That Met QC Criteria
October 11, 2018
First Posted (Actual)
October 12, 2018
Study Record Updates
Last Update Posted (Actual)
October 12, 2018
Last Update Submitted That Met QC Criteria
October 11, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- TJ-10207102
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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