TSIHi: Incidence and Risk Factors for TSIH

Sponsor
Hospital de Mataró (Other)
Overall Status
Completed
CT.gov ID
NCT04410744
Collaborator
(none)
76
7

Study Details

Study Description

Brief Summary

Trocar site incisional hernia (TSIH) is the most frequent complication associated to laparoscopic surgery. Few studies currently describes its real prevalence or risk factors. The aim of this study is to determine the real incidence of TSIH and to identify risk factors in the investigator's series of patients.

A cross sectional, prospective study is performed including consecutive patients who underwent a laparoscopic procedure during a four months period. All the patients are assessed both clinically (TSIHc) and by an ultrasonographic exam (TSIHu). Main variable studied is the incidence of TSIH. A multivariate analysis is performed to identify risk factors.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Ultrasonographic examination

Detailed Description

Single-centre cross-sectional study based on prospective clinical and radiological assessment and retrospective risk factor analyses performed at a single hospital.

All consecutive patients who underwent laparoscopic surgery (cholecystectomy, colon resection, adrenalectomy, Nissen fundoplication and appendectomy) during a four months period were included in the study. At least 30 months after hospital discharge, they were invited by telephone to participate in the study. Detailed project information was provided, and those who accepted received an appointment for an outpatient visit and a dynamic ultrasound. Informed consent was obtained from all participants. In all patients, the umbilical trocar wound was closed with an interrupted suture with synthetic braided absorbable 2/0 suture (Novosyn® or Safil®). During the postoperative outpatient visit, clinical and ultrasonographic examinations were performed. To increase study homogeneity, all clinical examinations and ultrasounds were performed by a single surgeon and a single radiology resident supervised by the same abdominal radiology consultant, respectively. Sonography was performed with an Applio 500 equipment (Toshiba, Japan) with a 3.5MHz convex probe and a 7MHz linear probe. The ultrasound diagnosis was based on the identification of an abdominal wall defect with intraabdominal tissue protrusion. The main variables of the study were clinical (TSIHc) and ultrasound (TSIHu) diagnosis of incisional hernia. All results and variables were introduced in a previous specifically designed database (File MakerPro 11.0v3 © 1984-2011 FileMaker, Inc.). Data were collected from clinical interviews, physical and radiological examinations and the electronic medical record. Statistical analyses were performed using the SPSS statistical software (IBM SPSS® Statistics).

Study Design

Study Type:
Observational
Actual Enrollment :
76 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Incidence and Risk Factors for Trocar Site Incisional Hernia Detected by Clinical and Ultrasonographic Examination.
Actual Study Start Date :
Jun 2, 2015
Actual Primary Completion Date :
Jan 1, 2016
Actual Study Completion Date :
Jan 1, 2016

Outcome Measures

Primary Outcome Measures

  1. clinical TSIH incidence [30 seconds]

    Presence / absence palpableTSIH (yes / not)

  2. ultrasonographic TSIH incidence [1 minute 30 seconds]

    Identification of an abdominal wall defect with intraabdominal tissue protrusion (yes /not) Caudal and cranial diameters of the abdominal wall's defect (cm)

Secondary Outcome Measures

  1. Risk factors for TSIH [5 minutes]

    Risk factors for TSIH determination. Information obtained from the electronic medical record

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Previous laparoscopic surgery

  • Age ≥18 years

  • Informed consent signed

Exclusion Criteria:
  • Previous umbilical hernia repair

  • Age < 18 years

  • Informed consent not signed

  • Failure to attend the postoperative appointment

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hospital de Mataró

Investigators

  • Principal Investigator: Ana Ciscar, Hospital de Mataró

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ana Ciscar, General and digestive surgery specialist, Hospital de Mataró
ClinicalTrials.gov Identifier:
NCT04410744
Other Study ID Numbers:
  • TSIH INCIDENCE
First Posted:
Jun 1, 2020
Last Update Posted:
Jun 4, 2020
Last Verified:
Jun 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ana Ciscar, General and digestive surgery specialist, Hospital de Mataró
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 4, 2020