Does Icodextrin Reduce the Risk of Small Bowel Obstruction?
Study Details
Study Description
Brief Summary
The study aims at investigating if icodextrin 4% instilled in abdominal cavity during surgery can reduce the risk of surgery and hospitalisation for small bowel obstruction in patients with colorectal cancer. Follow-up data is collected from the Swedish national colorectal cancer registry.Patients are followed for 5 years postoperatively.The study is a randomized Swedish multicenter study and planned to include 1,800 patients. A safety control is planned after 300 included patients.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Detailed Description
Icodextrin 7.5% is used in peritoneal dialysis. In animal models and in gynecological surgery a 4% solution of Icodextrin has been tested as a possible agent of reducing adhesions by acting as a barrier between peritoneal surfaces. Some data support a reduction af adhesions (van den Tool et al., Brown et al.). However, is not known whether icodextrin reduces the need for surgery or hospitalisation for small bowel obstruction.This study aims to study these parameters as well as complications and survival.
Patients with colorectal cancer and scheduled for surgery with curative intent will be (after patients acceptance) randomized to have icodextrin 4% instilled in the abdominal cavity or not. Patients allocated to icodextrin arm will have 100 ml of icodextrin 4% instilled every 30 minutes during surgery and at end of operation further 1000 ml instilled in the abdominal cavity. Postoperative care is performed according to each hospital praxis.
Follow-up data will be collected from the Swedish National Colorectal cancer registry. Data 30 days postoperatively will be analysed for early small bowel obstruction and other early complications. The study ends 5 years postoperatively with analysis of surgery and hospitalization for small bowel obstruction as well as survival and longterm complications.
A safety analysis is planned after the first 300 randomized patients with respect to early (30 days) complications. These data will analysed blindly by external reviewers.
Randomization (1:1) will be performed at the Regional Cancer Centrum in the Uppsala-Örebro region. The study aims to randomise 1800 patients.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Surgery and Icodextrin Icodextrin 4% instilled every 30 minutes during surgery and 1000 ml instilled before closure of abdomen |
Procedure: Surgery
Drug: Icodextrin
|
Active Comparator: Surgery No instillations during surgery |
Procedure: Surgery
|
Outcome Measures
Primary Outcome Measures
- Surgery for small bowel obstruction [5 years]
The proportion of patients that have undergone surgery for small bowel obstruction will be compared between the groups.
Secondary Outcome Measures
- Hospitalisation for small bowel obstruction [5 years]
- Overall and cancer survival [5 years]
- Postoperative complications [30 days]
Safety control of first 300 randomised patients
- Postoperative complications [30 days]
For all randomised patients
Eligibility Criteria
Criteria
Inclusion Criteria:
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Colorectal cancer
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Curative surgery planned
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Informed consent
-
Age 18-85
Exclusion Criteria:
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Local surgery planned
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Generalized disease
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Other malignancy
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Not informed consent
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Eskilstuna Hospital | Eskilstuna | Sweden | ||
2 | Falun Hospital | Falun | Sweden | ||
3 | Gävle Hospital | Gävle | Sweden | ||
4 | Jönköping Hospital | Jönköping | Sweden | ||
5 | Karlstad Hospital | Karlstad | Sweden | ||
6 | Lidköping Hospital | Lidköping | Sweden | ||
7 | Luleå Hospital | Luleå | Sweden | ||
8 | Mora Hospital | Mora | Sweden | ||
9 | Norrrköping Hospital | Norrköping | Sweden | ||
10 | Nyköping Hospital | Nyköping | Sweden | ||
11 | Torsby Hospital | Torsby | Sweden | ||
12 | University Hospital | Uppsala | Sweden | ||
13 | Västerås Hospital | Västerås | Sweden |
Sponsors and Collaborators
- Uppsala University
Investigators
- Principal Investigator: Urban Karlbom, PhD, University Hospital, Uppsala
- Study Director: Lars Påhlman, Professor, University Hospital
Study Documents (Full-Text)
None provided.More Information
Publications
- Brown CB, Luciano AA, Martin D, Peers E, Scrimgeour A, diZerega GS; Adept Adhesion Reduction Study Group. Adept (icodextrin 4% solution) reduces adhesions after laparoscopic surgery for adhesiolysis: a double-blind, randomized, controlled study. Fertil Steril. 2007 Nov;88(5):1413-26. Epub 2007 Mar 26.
- van den Tol P, ten Raa S, van Grevenstein H, Marquet R, van Eijck C, Jeekel H. Icodextrin reduces postoperative adhesion formation in rats without affecting peritoneal metastasis. Surgery. 2005 Mar;137(3):348-54.
- Dnr 2009/123