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ID
Source
Brief title
Health condition
Abdominal surgery, midline incisions, suture technique, incisional hernia, burst abdomen, wound infection
Sponsors and support
Intervention
Outcome measures
Primary outcome
Incisional hernia occurence within one year clinically and/or radiographically detected.
Secondary outcome
1. Postoperative complications => burst abdomen and wound infection;
2. Pain;
3. Quality of life;
4. Cost effectiveness.
Background summary
Incisional hernia is the most common complication after abdominal surgery with a reported incidence of
up to 15% at 1 year follow-up. In The Netherlands, 100.000 laparotomies and 4000 incisional hernia
repairs are performed annually. The costs of hernia repair (4 kEuro) hence amount to over 16 million
euro. Moreover, many patients with incisional hernia are not re-operated due to anticipated recurrence
rates of 30-60%. The major factor for development of incisional hernia is the surgical wound failure due
to insufficient suture techniques. The latter complication, which occurs in 1-4% of abdominal surgery,
involves bursting of the abdominal wound and the muscle layers, which causes the intestines to
protrude from the incision. It is associated with a high incidence of surgical site infections, prolonged
hospital stay and high mortality rates.
Recent clinical and experimental data suggest that a relatively new technique with many small tissue
bites should be more effective in the prevention of incisional hernia when compared to the standard
large bite technique.
We propose a multicenter double blind RCT to compare the routinely used large bite technique with the
small bites technique.
Objective of the study:
Primary question:
1. Which bite size should be used to close a midline incision to prevent incisional hernia?
Secondary questions:
2. Is there a difference in postoperative complications between the two patient groups?
3. Is there a difference in postoperative pain between the two patient groups?
4. Is there a difference in postoperative quality of life between the two patient groups?
5. Is it cost-effective to use the small bites technique?
The trial will be a double blinded randomized controlled prospective trial, in which the large bites
technique will be compared with the small bites technique. Patients will be preoperatively randomized in
two groups to either receive closure with the large tissue bites technique or with the small tissue bites
technique. Patients will be kept unaware of the procedure until the endpoint of the trial. Surgeons or
surgical residents and radiologists blinded for the procedure will do outpatient clinic controls.
Study population:
550 surgical patients who will undergo a midline laparotomy will be asked to join this study.
Study objective
Recent clinical and experimental data suggest that a relatively new technique with many small tissue
bites should be more effective in the prevention of incisional hernia when compared to the standard
large bite technique.
We propose a multicenter double blind RCT to compare the routinely used large bite technique with the
small bites technique.
Study design
At 1 and 12 months, a clinical examination and ultrasound examination will be performed by an examiner blinded to the procedure to examine the midline for any (a-)symptomatic incisional hernias.
Participating patients will be asked to fill in booklets containing quality of life questionnaires before surgery and at 1, 3, 6 and 12 months after surgery.
Intervention
In one group of 275 patients the conventional large bites technique will be applied with bites widths of
1,5 cm and inter suture spacing of 1 cm with the use of slowly absorbable 1-0 double loop suture
material with a 48 mm needle.
In the other group of 275 patients the small bites technique will be applied with bite widths of 0,5 cm
and inter suture spacing of 0,5 cm with the use of slowly absorbable 2-0 single suture material with a
36 mm needle only in the linea alba. In the small bites technique there will be twice as many stitches
with a smaller needle and thinner suture material.
E.B. Deerenberg
Rotterdam 3000 CA
The Netherlands
+31 (0)6 33335280
stitchtrial@erasmusmc.nl
E.B. Deerenberg
Rotterdam 3000 CA
The Netherlands
+31 (0)6 33335280
stitchtrial@erasmusmc.nl
Inclusion criteria
1. Signed informed consent;
2. Midline incision;
3. Age >= 18 years.
Exclusion criteria
1. Previous midline incision within 3 months before surgery;
2. Previous incisional hernia or burst;
3. Abdoman after a midline incision;
4. Pregnancy.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
NTR-new | NL1935 |
NTR-old | NTR2052 |
Other | MEC/NL : 2009-026/26225.078.09 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |