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Endostomal Three-dimensional Ultrasonography for Parastomal Hernia (CTULOP)

Primary Purpose

Parastomal Hernia

Status
Unknown status
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Endostomal three-dimensional ultrasonography
Computerized tomography of the abdomen
Clinical examination
Evaluation at laparotomy/laparoscopy
Sponsored by
Umeå University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Parastomal Hernia focused on measuring Parastomal hernia, Ultrasound, Ultrasonography, Endostomal, Intrastomal, Colostomy, Ileostomy

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • End colostomy or end ileostomy since ≥ 1 year
  • Planned for laparotomy or laparoscopy
  • Age ≥ 18
  • Speaks and reads Swedish language
  • Informed consent

Exclusion Criteria:

  • Known parastomal hernia only indication for laparotomy or laparoscopy

Sites / Locations

  • Sunderby HospitalRecruiting
  • Södertälje Hospital
  • University Hospital of UmeåRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

All patients

Arm Description

All patients undergo endostomal three-dimensional ultrasonography, computerized tomography, clinical examination and laparotomy/laparoscopy. At all the respective examinations, the presence of a parastomal hernia as well as hernia location and size is evaluated.

Outcomes

Primary Outcome Measures

Test characteristics
Sensitivity, specificity, predictive values, likelihood ratio

Secondary Outcome Measures

Full Information

First Posted
March 12, 2020
Last Updated
November 2, 2020
Sponsor
Umeå University
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1. Study Identification

Unique Protocol Identification Number
NCT04311333
Brief Title
Endostomal Three-dimensional Ultrasonography for Parastomal Hernia
Acronym
CTULOP
Official Title
Endostomal Three-dimensional Ultrasonography Compared to Clinical Examination, Computerized Tomography and Intraoperative Findings for Parastomal Hernia Diagnosis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
September 27, 2016 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Umeå University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The intention is to examine the role of ultrasonographic examination inside intestinal stomas in diagnosing parastomal hernia. Patients with a stoma since at least one year back who are being scheduled for abdominal surgery will be examined for eligibility according to the selection criteria. Included patients will undergo routine clinical examination, endostomal ultrasonography and computerized tomography scan of the abdomen. Findings will be correlated to findings during surgery (gold standard). Values for sensitivity, specificity, predictive values and likelihood ratio will be calculated.
Detailed Description
Parastomal hernia (PSH) is one of the most common stoma complications, with an incidence of 30-50 % within just a couple of years of stoma creation. Surgical parastomal hernia repair is a morbid and complicated procedure, with a 30-day reoperation rate of 13 % and 30-day mortality rate of 6 % in population-based surveys. There is no established gold standard diagnostic modality. Routinely, patients are examined clinically in various positions with and without increased intra-abdominal pressure. It has been shown in previous studies that clinical examination has a very low inter-observer reliability. Computerized tomography is often performed in addition to clinical examination, but is not ideal in diagnosing PSH either, not only beacause of insufficient test characteristics but also since the examinations should ideally be performed with specific protocols, prone position and be reviewed by a dedicated radiologist. The risk of incorrectly diagnosing a PSH (false positive) is that patients might subsequently be exposed to complex and dangerous surgical interventions without any health benefit, while incorrectly ruling out a PSH (false negative) can cause the patient to have to live with potentially treatable symptoms, life-threatening bowel incarceration being the most severe potential complication. Thus, improved diagnostic accuracy is required. A method that has been developed within our research group is endostomal tree-dimensional ultrasonography, which has preliminarily proven to be approximately as sensitive as CT, with a markedly higher specificity. A larger and less selected study needs to be conducted in order to reliably calculate test characteristics, predictive values and likelihood ratio.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parastomal Hernia
Keywords
Parastomal hernia, Ultrasound, Ultrasonography, Endostomal, Intrastomal, Colostomy, Ileostomy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All patients will be examined with endostomal three-dimensional ultrasonography, clinical examination and computerized tomography before undergoing laparotomy or laparoscopy
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
All patients
Arm Type
Experimental
Arm Description
All patients undergo endostomal three-dimensional ultrasonography, computerized tomography, clinical examination and laparotomy/laparoscopy. At all the respective examinations, the presence of a parastomal hernia as well as hernia location and size is evaluated.
Intervention Type
Diagnostic Test
Intervention Name(s)
Endostomal three-dimensional ultrasonography
Intervention Description
Examination with rectal probe enclosed by water-filled balloon. Rectal mode. Dynamic examination in different positions with and without increased intra-abdominal pressure.
Intervention Type
Diagnostic Test
Intervention Name(s)
Computerized tomography of the abdomen
Intervention Description
Supine position, without increased intra-abdominal pressure. Experienced radiologist interprets the examination. If adequate examination has already been performed within the last 10 months, these images will be used and the patient will thus not undergo computerized tomography within the study.
Intervention Type
Diagnostic Test
Intervention Name(s)
Clinical examination
Intervention Description
Patients will be clinically examined with inspection and palpation in supine and erect position with and without increased intra-abdominal pressure.
Intervention Type
Diagnostic Test
Intervention Name(s)
Evaluation at laparotomy/laparoscopy
Intervention Description
During laparotomy or laparoscopy, inspection and/or palpation of the stoma at the abdominal wall orifice is performed.
Primary Outcome Measure Information:
Title
Test characteristics
Description
Sensitivity, specificity, predictive values, likelihood ratio
Time Frame
≥ 1 year since stoma creation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: End colostomy or end ileostomy since ≥ 1 year Planned for laparotomy or laparoscopy Age ≥ 18 Speaks and reads Swedish language Informed consent Exclusion Criteria: Known parastomal hernia only indication for laparotomy or laparoscopy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Johan Nyman, M.D.
Phone
(+46)90 786 46 87
Email
johan.nyman@umu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Karin Strigård, M.D., Ph.D.
Phone
(+46)90 786 46 87
Email
karin.strigård@umu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Karin Strigård
Organizational Affiliation
Department of Surgical and Perioperative Sciences, Umeå University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunderby Hospital
City
Luleå
State/Province
Norrbotten County
ZIP/Postal Code
971 80
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Johan Nyman, M.D.
Phone
+46727436345
Email
johan.nyman@umu.se
First Name & Middle Initial & Last Name & Degree
Karin Strigård, M.D., Ph.D.
Phone
+46907864687
Email
karin.strigard@umu.se
Facility Name
Södertälje Hospital
City
Södertälje
State/Province
Stockholm
ZIP/Postal Code
152 86
Country
Sweden
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fredrik Brännström, M.D., Ph.D.
Phone
+46855024000
Email
fredrikbrannstrom@yahoo.se
Facility Name
University Hospital of Umeå
City
Umeå
State/Province
Västerbotten County
ZIP/Postal Code
907 37
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Johan Nyman, M.D.
Phone
+46727436345
Email
johan.nyman@umu.se
First Name & Middle Initial & Last Name & Degree
Karin Strigård, M.D., Ph.D.
Phone
+46907864687
Email
karin.strigard@umu.se

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20821218
Citation
Gurmu A, Matthiessen P, Nilsson S, Pahlman L, Rutegard J, Gunnarsson U. The inter-observer reliability is very low at clinical examination of parastomal hernia. Int J Colorectal Dis. 2011 Jan;26(1):89-95. doi: 10.1007/s00384-010-1050-2. Epub 2010 Sep 7.
Results Reference
background
PubMed Identifier
21509751
Citation
Gurmu A, Gunnarsson U, Strigard K. Imaging of parastomal hernia using three-dimensional intrastomal ultrasonography. Br J Surg. 2011 Jul;98(7):1026-9. doi: 10.1002/bjs.7505. Epub 2011 Apr 20.
Results Reference
background
PubMed Identifier
22772711
Citation
Strigard K, Gurmu A, Nasvall P, Pahlman P, Gunnarsson U. Intrastomal 3D ultrasound; an inter- and intra-observer evaluation. Int J Colorectal Dis. 2013 Jan;28(1):43-7. doi: 10.1007/s00384-012-1526-3. Epub 2012 Jul 7.
Results Reference
background
PubMed Identifier
24986139
Citation
Nasvall P, Wikner F, Gunnarsson U, Rutegard J, Strigard K. A comparison between intrastomal 3D ultrasonography, CT scanning and findings at surgery in patients with stomal complaints. Int J Colorectal Dis. 2014 Oct;29(10):1263-6. doi: 10.1007/s00384-014-1944-5. Epub 2014 Jul 2.
Results Reference
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Learn more about this trial

Endostomal Three-dimensional Ultrasonography for Parastomal Hernia

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