Does Icodextrin Reduce the Risk of Small Bowel Obstruction?

Sponsor
Uppsala University (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02318888
Collaborator
(none)
1,808
13
2
156
139.1
0.9

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

Study Type:
Interventional
Actual Enrollment :
1808 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Does Icodextrin Reduce the Risk of Small Bowel Obstruction?
Actual Study Start Date :
Dec 1, 2009
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

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

  1. 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

  1. Hospitalisation for small bowel obstruction [5 years]

  2. Overall and cancer survival [5 years]

  3. Postoperative complications [30 days]

    Safety control of first 300 randomised patients

  4. Postoperative complications [30 days]

    For all randomised patients

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 85 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Colorectal cancer

  • Curative surgery planned

  • Informed consent

  • Age 18-85

Exclusion Criteria:
  • Local surgery planned

  • Generalized disease

  • Other malignancy

  • 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

Responsible Party:
Uppsala University
ClinicalTrials.gov Identifier:
NCT02318888
Other Study ID Numbers:
  • Dnr 2009/123
First Posted:
Dec 17, 2014
Last Update Posted:
Mar 31, 2020
Last Verified:
Mar 1, 2020
Keywords provided by Uppsala University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 31, 2020