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Optimised Recovery With Accelerated Nutrition and GI Enhancement (ORANGE)

Primary Purpose

Colorectal Liver Metastases

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Post operative laxation (Magnesium Oxide)
Preoperative metabolic conditioning postoperative nutritional supplementation
Standard ERAS group
Sponsored by
University of Edinburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Colorectal Liver Metastases focused on measuring Perioperative, recovery, nutrition, enhanced, laxative

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients undergoing hepatic resection for benign or malignant conditions
  • Able to understand the nature of the study and what will be required of them.
  • Men and non-pregnant, non-lactating women
  • BMI 18 - 30

Exclusion Criteria:

  • Inability to give written, informed consent
  • Patients with dementia or neurological impairment
  • Patients with pre-existing condition limiting mobility
  • Planned bile duct excision
  • Repeat or staged procedures
  • Central extended resections
  • Underlying cirrhotic liver disease
  • Jaundice (Bilirubin > 50 μmol/L)

Sites / Locations

  • University Hospital Maastricht
  • Edinburgh Royal Infirmary

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Experimental

Experimental

Arm Label

1

2

3

4

Arm Description

Follow a standard Enhanced Recovery After Surgery protocol

Follow a standard Enhanced Recovery After Surgery protocol and will receive 1 g of Magnesium Oxide laxative twice daily from the day after surgery until discharge

Follow a standard Enhanced Recovery After Surgery protocol and will receive preconditioning with carbohydrate and fluid loading prior to surgery (800ml of Nutricia Preop the evening before surgery and 400 the morning of surgery 2 hours prior to anaesthesia) and postoperative nutritional supplements (200 ml Nutricia Fortisip twice daily) after surgery for 30 days

Follow a standard Enhanced Recovery After Surgery protocol and will receive preconditioning with carbohydrate and fluid loading prior to surgery (800ml of Nutricia Preop the evening before surgery and 400 the morning of surgery 2 hours prior to anaesthesia) and postoperative nutritional supplements (200 ml Nutricia Fortisip twice daily) after surgery for 30 days and will receive postoperative laxative in the form of 20 ml of Magnesium Oxide twice daily form the day after surgery until discharge

Outcomes

Primary Outcome Measures

Recovery of gastrointestinal function: Time to pass flatus/stool (hours following the end of surgery)

Secondary Outcome Measures

t ½ Gastric emptying time on the morning of post-operative day 3
Length of hospital stay: nights spent in hospital post-op
Patient activity level: measured by activPAL® activity meter

Full Information

First Posted
October 2, 2007
Last Updated
November 4, 2010
Sponsor
University of Edinburgh
Collaborators
NHS Lothian
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1. Study Identification

Unique Protocol Identification Number
NCT00538954
Brief Title
Optimised Recovery With Accelerated Nutrition and GI Enhancement
Acronym
ORANGE
Official Title
A Randomised Controlled Trial of Optimised Surgical Recovery: the Potential Synergy Between Enhanced Gastrointestinal Motility and Oral Nutritional/ Metabolic Support
Study Type
Interventional

2. Study Status

Record Verification Date
October 2007
Overall Recruitment Status
Completed
Study Start Date
August 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Edinburgh
Collaborators
NHS Lothian

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Factors which delay recovery following uncomplicated abdominal surgery include uncontrolled pain, intolerance of diet and poor mobility. Enhanced recovery after Surgery (ERAS) programmes are perioperative care pathways that address systematically these issues (i.e. improved dynamic pain relief, optimised nutritional care and enforced mobilisation) to promote a faster recovery and a shorter stay. The key treatments that improve outcome within an ERAS programme are not known. Moreover there are few acceptable, objective endpoints to assess key outcome variables such as return of GI function. This randomised trial will assess the potential synergy between early recovery of GI function (laxation) and early postoperative oral nutritional support(with associated preoperative preconditioning using carbohydrate/fluid loading). The main overall outcome targets being improved recovery of gastrointestinal function, postoperative nutritional status and physical function. It will validate the use of a novel, objective technique to measure gastric motility (surrogate for GI function). Such refinement of ERAS should result in shorter hospital stay and better use of limited health care resource.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Liver Metastases
Keywords
Perioperative, recovery, nutrition, enhanced, laxative

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
64 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Follow a standard Enhanced Recovery After Surgery protocol
Arm Title
2
Arm Type
Experimental
Arm Description
Follow a standard Enhanced Recovery After Surgery protocol and will receive 1 g of Magnesium Oxide laxative twice daily from the day after surgery until discharge
Arm Title
3
Arm Type
Experimental
Arm Description
Follow a standard Enhanced Recovery After Surgery protocol and will receive preconditioning with carbohydrate and fluid loading prior to surgery (800ml of Nutricia Preop the evening before surgery and 400 the morning of surgery 2 hours prior to anaesthesia) and postoperative nutritional supplements (200 ml Nutricia Fortisip twice daily) after surgery for 30 days
Arm Title
4
Arm Type
Experimental
Arm Description
Follow a standard Enhanced Recovery After Surgery protocol and will receive preconditioning with carbohydrate and fluid loading prior to surgery (800ml of Nutricia Preop the evening before surgery and 400 the morning of surgery 2 hours prior to anaesthesia) and postoperative nutritional supplements (200 ml Nutricia Fortisip twice daily) after surgery for 30 days and will receive postoperative laxative in the form of 20 ml of Magnesium Oxide twice daily form the day after surgery until discharge
Intervention Type
Drug
Intervention Name(s)
Post operative laxation (Magnesium Oxide)
Intervention Description
20 ml of Magnesium Oxide twice daily from the day after surgery until discharge
Intervention Type
Dietary Supplement
Intervention Name(s)
Preoperative metabolic conditioning postoperative nutritional supplementation
Intervention Description
Nutricia PreOP drinks 800 ml between 8-10 pm the evening before surgery Nutricia PreOP drinks 400 ml completed 2 hours before anaesthesia on the morning of surgery Nutricia Fortisip drinks 2 x 200 ml drinks from the day after surgery until day 30
Intervention Type
Other
Intervention Name(s)
Standard ERAS group
Primary Outcome Measure Information:
Title
Recovery of gastrointestinal function: Time to pass flatus/stool (hours following the end of surgery)
Time Frame
Number of hours post surgery
Secondary Outcome Measure Information:
Title
t ½ Gastric emptying time on the morning of post-operative day 3
Time Frame
Postoperative day 3
Title
Length of hospital stay: nights spent in hospital post-op
Time Frame
Until discharge
Title
Patient activity level: measured by activPAL® activity meter
Time Frame
postoperative day 2 - 7 and day 30 - 37

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients undergoing hepatic resection for benign or malignant conditions Able to understand the nature of the study and what will be required of them. Men and non-pregnant, non-lactating women BMI 18 - 30 Exclusion Criteria: Inability to give written, informed consent Patients with dementia or neurological impairment Patients with pre-existing condition limiting mobility Planned bile duct excision Repeat or staged procedures Central extended resections Underlying cirrhotic liver disease Jaundice (Bilirubin > 50 μmol/L)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul Hendry, MBChB
Organizational Affiliation
University of Edinburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Maastricht
City
Maastricht
Country
Netherlands
Facility Name
Edinburgh Royal Infirmary
City
Edinburgh
ZIP/Postal Code
EH16 4SA
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
20602497
Citation
Hendry PO, van Dam RM, Bukkems SF, McKeown DW, Parks RW, Preston T, Dejong CH, Garden OJ, Fearon KC; Enhanced Recovery After Surgery (ERAS) Group. Randomized clinical trial of laxatives and oral nutritional supplements within an enhanced recovery after surgery protocol following liver resection. Br J Surg. 2010 Aug;97(8):1198-206. doi: 10.1002/bjs.7120.
Results Reference
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Optimised Recovery With Accelerated Nutrition and GI Enhancement

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