Suture Techniques to Reduce the Incidence of Incisional Hernia: LTFU STITCH Trial (LTFU-STITCH)

Suture Techniques to Reduce the Incidence of Incisional Hernia After Midline Laparotomy; Long-Term Follow-Up of the STITCH Trial

Rationale: Incisional hernias (IH) are a frequent complication after abdominal surgery. Prevalence of an IH varies depending on the previous abdominal procedure but could be as high as 70% in high-risk patients after open surgery. To investigate different fascia closure techniques in the prevention of IHs, the STITCH trial (NCT01132209) was designed. The study compared two different closure techniques for closure of a midline incision in adult patients undergoing an elective abdominal laparotomy. Patients were randomly assigned to the intervention group (small bites 5 mm x 5 mm) or the control group (large bites 1 cm x 1 cm). The study showed that small bites are much more effective than large bites in the prevention of an incisional hernia when closing a midline incision.

So far, it has not been studied whether there is still a long-term difference in incidence of incisional hernia between the small bites and the large bites group.

Objective: The primary objective of this study is to determine the difference in incidence of IH between the small bites and the large bites group after 10 years of follow-up from time of randomization in the STITCH trial. The secondary objectives are to measure quality of life (QoL), body image and cosmetic results, and abdominal wall function through questionnaires and physical examination in those patients who are still alive.

Study Overview

• Status: Recruiting
• Conditions: Quality of Life; Pain; Surgery; Wound Infection; Incisional Hernia; Fascial Dehiscence
• Intervention / Treatment: Procedure: Small bites technique; Procedure: Conventional large bites closure

Detailed Description

Rationale: Incisional hernias (IH) are a frequent complication after abdominal surgery. Prevalence of an IH varies depending on the previous abdominal procedure but could be as high as 70% in high-risk patients after open surgery. To investigate different fascia closure techniques in the prevention of IHs, the STITCH trial (NCT01132209) was designed, a randomized controlled trial in which 560 patients were included between October 2009 and March 2012. The study compared two different closure techniques for closure of a midline incision in adult patients undergoing an elective abdominal laparotomy. Patients were randomly assigned to the intervention group (small bites 5 mm x 5 mm) or the control group (large bites 1 cm x 1 cm). It showed that small bites are much more effective than large bites in the prevention of an incisional hernia when closing a midline incision.

So far, it has not been studied whether there is still a long-term difference in incidence of incisional hernia between the small bites and the large bites group.

Objective: The primary objective of this study study is to determine the difference in incidence of IH between the small bites and the large bites group after 10 years of follow-up from time of randomization in the STITCH trial. The secondary objectives are to measure quality of life (QoL), body image and cosmetic results, and abdominal wall function through questionnaires and physical examination in those patients who are still alive.

Study design: Assessment of long-term follow-up (10-13 years) of a randomized controlled multicenter study based on retrospective review of patient files and relevant imaging of the entire trial population, as well as questionnaires and physical and radiological examination of patient who are still alive.

Study population: Of the 560 included patients in the original STITCH trial, 545 completed the 1-year follow-up.

Intervention (if applicable): Not applicable. Main study parameters/endpoints: The primary outcome measure is the 10-year midline incisional hernia rate. The primary endpoint will be determined for the 545 patients of the original intention-to-treat population using Kaplan Meier analysis. In patients who died during follow-up, this will be evaluated by reviewing the available medical charts and radiological studies. CT-scans of the abdomen will be evaluated by the study-team. If CT imaging is not available, documented findings during physical examination by the relevant medical specialist will be considered. Patients being still alive with written informed consent to be contacted will be approached for their willingness to participate in this follow-up study, and after consent, we will reassess CT scans for an incisional hernia. All patients who are still alive and want to participate in this study will be asked to visit the hospital once for physical examination and an ultrasound of the abdominal wall.

Secondary outcome parameters include QoL and cosmetic outcome, Patients still alive with consent for participation will be sent the following questionnaires: MOS SF-36 and EQ-5D (QoL), Dresden Body Image Questionnaire (body image), Body Image Questionnaire (cosmesis), Hernia-Related Quality of Life Survey (abdominal wall function). Furthermore, readmission and surgical intervention rates related to midline IH will be determined for the entire study population.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Undergoing an ultrasound, physical examination and completing several questionnaires may be considered burdensome for the patient.

• Study Type: Interventional
• Enrollment (Estimated): 560
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Rudolf van den Berg; Phone Number: 0107043683; Email: R.vandenBerg.4@Erasmusmc.nl
• Study Contact Backup: Name: Sarah van Egmond; Phone Number: 0107043683; Email: S.vanEgmond@Franciscus.nl

Study Locations

• Netherlands
  • Amersfoort, Netherlands
    • Recruiting
    • Meander Medical Center
  • Arnhem, Netherlands
    • Recruiting
    • Rijnstate Ziekenhuis
  • Beverwijk, Netherlands
    • Recruiting
    • Red Cross Hospital
  • Gouda, Netherlands
    • Recruiting
    • Groene Hart Ziekenhuis
  • Haarlem, Netherlands
    • Recruiting
    • Spaarne Gasthuis
  • Rotterdam, Netherlands
    • Recruiting
    • Franciscus Gasthuis & Vlietland
  • Rotterdam, Netherlands
    • Recruiting
    • Prior Havenziekenhuis patients currently in the Erasmus MC
  • Tilburg, Netherlands
    • Recruiting
    • Elisabeth-TweeSteden Ziekenhuis
  • South-Holland
    • Rotterdam, South-Holland, Netherlands, 3015
      • Recruiting
      • Erasmus MC
      • Contact: Pieter J Tanis, Prof.dr; Phone Number: 003110 704 0704; Email: p.tanis@erasmusmc.nl

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

In order to be eligible to participate in this study, a subject must meet the following criteria:

• Available signed informed consent form for the original STITCH trial of the patients who are still alive.
• Or if the patients has died, the medical records are reviewed.

A potential subject who meets the following criteria will be excluded from participation in this study:

- Patients that on the original informed consent form of the STITCH trial, checked the box that they did not want to be approached for future follow-up studies.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Single

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Small bites suturing technique of the abdominal wall during midline laparotomy; In the experimental group of 288 patients the small bites technique was applied with bite widths of 0,5 cm and inter suture spacing of 0,5 cm with the use of PDS plus ll 2-0 single suture material with a 31 mm needle placed in the linea alba. In the small bites technique, twice as many stitches will be placed per sutured cm, with a smaller needle and thinner suture material.	Procedure: Small bites technique; Closure of the fascia after midline laparotomy using a slowly resorbalbe 2.0 suture, with 0.5 cm bites, and 0.5 cm between the stitches, at least resulting in a 1:4 wound length:suture length ratio.
Active Comparator: Large bites suturing technique of the abdominal wall during midline laparotomy; As control the conventional large bites technique (mass closure) was applied with bites widths of 1 cm and inter-suture spacing of 1 cm with the use of PDS plus ll 1-0 double loop suture material with a 48 mm needle.	Procedure: Conventional large bites closure; Closure of a midline laparotomy using a slowy resorbable thick suture (e.g. PDS loop) with large bites and large steps (>= 1 cm).

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incisional hernia occurrence (and timeto incisional hernia outcome).	Incisional hernia occurrence after operation clinical and/or radiological diagnosis.	Patients will have a follow-up of up to 12 years, with most patients having a follow-up between 10 and 12 years.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Quality of life of the patient.	Quality of life measured by MOS SF-36, ranging from 0 (worst) to 100 (best).	Patients will have a follow-up of more than 10 years.
Quality of life of the patient.	Quality of life measured by and EQ-5D, ranging from 0 (worst) to 100 (best).	Patients will have a follow-up of up to 12 years.
Body image.	Body image measured by Dresden Body Image Questionnaire (DBIQ), consisting of 35 questions that can be answered with a yes or no. This results in a range of 0 (worst) to 35 (best) points.	Patients will have a follow-up of up to 12 years.
Cosmetic results, cosmesis.	Cosmetic results measured by Body Image Questionnaire (BIQ), consisting of 10 questions with a score ranging from 10 (worst) to 64 (best) points.	Patients will have a follow-up of up to 12 years.
AWF.	Hernia-Related Quality of Life Survey (HerQLes), with 12 questions ranging from 12 (worst) to 72 (best) points.	Patients will have a follow-up of up to 12 years.

Collaborators and Investigators

• Sponsor: Erasmus Medical Center
• Collaborators: Elisabeth-TweeSteden Ziekenhuis; Rijnstate Hospital; Red Cross Hospital Beverwijk; Spaarne Gasthuis; Meander Medisch Centrum; Franciscus &Vlietland
• Investigators: Principal Investigator: Pieter J Tanis, Erasmus Medical Center

Publications and helpful links

Helpful Links

• Original STITCH trial

Study record dates

Study Major Dates

• Study Start (Actual): August 1, 2023
• Primary Completion (Estimated): March 1, 2024
• Study Completion (Estimated): October 1, 2024

Study Registration Dates

• First Submitted: September 1, 2023
• First Submitted That Met QC Criteria: September 27, 2023
• First Posted (Actual): October 4, 2023

Study Record Updates

• Last Update Posted (Actual): October 4, 2023
• Last Update Submitted That Met QC Criteria: September 27, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Keywords: Pathologic Processes; Quality of Life; Pain; Surgery; Infections; Postoperative Complications; Wound Infection; Pathological Conditions, Anatomical; Incisional Hernia; Fascial Dehiscence
• Additional Relevant MeSH Terms: Pathologic Processes; Postoperative Complications; Pathological Conditions, Anatomical; Infections; Hernia; Wound Infection; Incisional Hernia
• Other Study ID Numbers: 9354 (Other Identifier: CTEP); IIS WC-2022-06 (Other Grant/Funding Number: Ethicon Inc.); MEC 2022-0652 (Registry Identifier: METC)

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