When Closing Midline Incisions, do Small Stitches Reduce the Risk for Incisional Hernia, Wound Infection or Dehiscence?

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00508053
Recruitment Status : Completed
First Posted : July 27, 2007
Last Update Posted : July 30, 2007
Information provided by:
Sundsvall Hospital

Brief Summary:
The purpose of this study is to determine whether a technique using very small stitches when closing a midline incision can reduce the risk for wound complications such as incisional hernia, infection or dehiscence.

Condition or disease Intervention/treatment Phase
Wound Infection Incisional Hernia Wound Dehiscence Procedure: Small stitches Procedure: Mass closure Not Applicable

Detailed Description:
Most abdominal surgical operations are made through a midline incision and 10% of the patients may get a wound infection. Infection is a risk factor for incisional hernia, which 12 months after the operation can be seen in 10-20% of the patients. Wound dehiscence is seen in approximately 1% of the patients. Surgery because of incisional hernias are common and in Sweden approximately 2000 patients per year needs an operation creating big costs. We know that a midline incision should be closed using a continuous technique, with a suture length to wound length ratio over 4. An earlier interventional study at the Surgical Department in Sundsvall showed that using that technique reduced the risk for hernia with 50%. Subsequent experimental studies indicates that the suture length to wound length ratio should be obtained by small stitches, placed close to each other only incorporating the aponeurosis, and not by large stitches incorporating the complete abdominal wall (mass closure). The hypothesis that midline incisions should be closed with small stitches only incorporating the aponeurosis has to be tested in a clinical trial.

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 737 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double
Primary Purpose: Prevention
Study Start Date : January 2001
Actual Study Completion Date : July 2007

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Active Comparator: 1
Mass closure
Procedure: Mass closure
Experimental: 2
Small stitches
Procedure: Small stitches

Primary Outcome Measures :
  1. Frequency of wound infection [ Time Frame: Within the first 30 days after surgery ]
  2. Frequency of incisional hernia [ Time Frame: One year after surgery ]

Secondary Outcome Measures :
  1. Frequency of wound dehiscence [ Time Frame: Within the first 10 days after surgery ]
  2. Effect of different suture techniques on wound complications related to patient characteristics such as age, BMI, sex etc. and operative characteristics such as emergency surgery, type of surgery, degree of contamination, surgeon,etc.. [ Time Frame: Within 1 year. ]

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.

Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Male or female patient with an acute or planned operation trough a midline incision at the Surgical Department in Sundsvall, Sweden

Exclusion Criteria:

  • Age under 18
  • Previous surgery through a midline incision
  • Scars from previous surgery crossing the midline
  • Preexisting hernia in the midline (umbilical, epigastric)

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT00508053

Sundsvall Hospital
851 86 Sundsvall, Sweden
Sponsors and Collaborators
Sundsvall Hospital
Principal Investigator: Daniel Millbourn, MD Sundsvall Hospital

Publications automatically indexed to this study by Identifier (NCT Number): Identifier: NCT00508053     History of Changes
Other Study ID Numbers: 2-Millbourn
First Posted: July 27, 2007    Key Record Dates
Last Update Posted: July 30, 2007
Last Verified: July 2007

Keywords provided by Sundsvall Hospital:
wound infection
incisional hernia
wound dehiscence
wound healing
postoperative complications
surgical techniques

Additional relevant MeSH terms:
Communicable Diseases
Wounds and Injuries
Wound Infection
Incisional Hernia
Pathological Conditions, Anatomical
Postoperative Complications
Pathologic Processes