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EDMONd - Elemental Diet in Bowel Obstruction (EDMONd)

Primary Purpose

Ovarian Cancer, Ovarian Neoplasms, Ovarian Disease

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Elemental 028 Extra Liquid
Sponsored by
Royal Surrey County Hospital NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Ovarian Cancer focused on measuring Feasibility, Elemental Diet, Quality of life, Palliative, Nutrition, Ovarian, Peritoneal, Advanced, Metastatic, Bowel obstruction, Inoperable

Eligibility Criteria

18 Years - 90 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age > 18 years
  • Confirmed inoperable bowel obstruction due to disseminated malignancy
  • Ability to tolerate 500ml of liquid
  • Capacity to give informed consent

Exclusion Criteria:

  • Bowel obstruction that can be managed with surgical intervention
  • Complete bowel obstruction and inability to tolerate small amount of liquid

Sites / Locations

  • Royal Surrey County Hospital NHS Foundation TrustRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Elemental 028 Extra Liquid

Arm Description

All patients will be assessed and given an individual plan for Elemental Diet (ED) introduction. The actual amount of ED prescribed will depend on the tolerance and palatability and not nutritional status. The recommendation of a minimum of 2 cartons of ED will be drunk orally by patients, along with other clear fluids only. Following introduction of ED, patients will be discharged from hospital (if applicable) and followed up for 2 weeks. They will have a telephone follow-up assessment once a week for 2 weeks. All other assessments will follow the standard of care. During the follow-up patients will be assessed using the Memorial Symptom Assessment Scale (MSAS) and will be asked to complete a nutritional diary every day and a quality of life questionnaire at several time points.

Outcomes

Primary Outcome Measures

Taste acceptability of ED
Taste of at least one flavor of ED graded as 2 out of 5 by patient on nutritional diary taste acceptability scale (1=I really like the taste, 2=I like the taste, 3=The taste is acceptable, 4=I do not like the taste but can drink it, 5=I do not like the taste and cannot drink it).
Change in incidence of vomiting
No deterioration in incidence of vomiting as measured on MSAS scale. Grading 1 (occurring rarely) or 2 (occurring occasionally) is acceptable. Deterioration considered as change to 3 (occurring frequently) or 4 (occurring almost constantly).
Change in incidence of pain
No deterioration in incidence of abdominal pain as measured on MSAS scale. Grading 1 (occurring rarely) or 2 (occurring occasionally) is acceptable. Deterioration considered as change to 3 (occurring frequently) or 4 (occurring almost constantly).

Secondary Outcome Measures

The number of patients who can tolerate ED following presentation with IBO and can subsequently be treated with palliative chemotherapy
Measured by reviewing hospital case notes
Number of patients alive at the end of the study
Measured by reviewing hospital case notes
Health related quality of life
Measured on EORTC-QLQ-C30
Nutritional intake
Measured by number of cartons taken by patient in 24 hours

Full Information

First Posted
April 3, 2017
Last Updated
March 25, 2019
Sponsor
Royal Surrey County Hospital NHS Foundation Trust
Collaborators
University of Surrey, Target Ovarian Cancer
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1. Study Identification

Unique Protocol Identification Number
NCT03150992
Brief Title
EDMONd - Elemental Diet in Bowel Obstruction
Acronym
EDMONd
Official Title
A Feasibility Study of Elemental Diet as an Alternative to Parenteral Nutrition for Patients With Inoperable Malignant Bowel Obstruction
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 19, 2017 (Actual)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Royal Surrey County Hospital NHS Foundation Trust
Collaborators
University of Surrey, Target Ovarian Cancer

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
A feasibility study to provide 'proof of concept' of Elemental Diet (ED) as an acceptable/ useful feeding option for patient with inoperable malignant bowel obstruction and to examine the impact of ED on quality of life
Detailed Description
The aim of this study is to determine whether Elemental Diet (a type of drink that contains an elemental protein source known as amino acids) can be tolerated by patients with inoperable bowel blockage who can no longer eat and are only able to swallow small amount of fluid. The objective is to find out whether elemental diet (ED) can be used as an acceptable nutrition and whether it improves the quality of life. Bowel blockage is a common complication in patients with ovarian cancer. Unfortunately when the cancer is advanced, this blockage can occur in many parts of the bowel therefore surgery is not possible. Every year in the UK some publications report the rate as high as 50% . One way to feed patients with bowel blockage is through the veins; this is known as parenteral nutrition (PN) however PN is rarely used in United Kingdom. Patients with malignant bowel blockage are often able to swallow small amounts of liquid but if they have no PN they are only able to survive for 2-3 weeks and the psychological as well as physical impact on patients and the family are very distressing. ED is a type of a drink which contains an elemental protein source known as amino acids. ED drinks are almost totally absorbed in the upper part of the bowel and therefore could be absorbed even in patients who have bowel blockage which usually develops lower down in the gut. If this study is successful and proves that ED can be tolerated and provide nutrition to patients with inoperable bowel blockage it will be a big step towards improving the quality of life at the final stage of cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ovarian Cancer, Ovarian Neoplasms, Ovarian Disease, Peritoneal Neoplasms, Peritoneal Diseases, Metastatic Ovarian Cancer, Primary Peritoneal Carcinoma, Abdominal Neoplasm, Bowel Obstruction
Keywords
Feasibility, Elemental Diet, Quality of life, Palliative, Nutrition, Ovarian, Peritoneal, Advanced, Metastatic, Bowel obstruction, Inoperable

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
34 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Elemental 028 Extra Liquid
Arm Type
Experimental
Arm Description
All patients will be assessed and given an individual plan for Elemental Diet (ED) introduction. The actual amount of ED prescribed will depend on the tolerance and palatability and not nutritional status. The recommendation of a minimum of 2 cartons of ED will be drunk orally by patients, along with other clear fluids only. Following introduction of ED, patients will be discharged from hospital (if applicable) and followed up for 2 weeks. They will have a telephone follow-up assessment once a week for 2 weeks. All other assessments will follow the standard of care. During the follow-up patients will be assessed using the Memorial Symptom Assessment Scale (MSAS) and will be asked to complete a nutritional diary every day and a quality of life questionnaire at several time points.
Intervention Type
Dietary Supplement
Intervention Name(s)
Elemental 028 Extra Liquid
Other Intervention Name(s)
Elemental Diet
Intervention Description
A nutritionally complete, liquid elemental diet consisting of a mixture of essential and non-essential amino acids, carbohydrate, fat, vitamins, minerals, trace elements and flavourings with sugars & sweeteners.
Primary Outcome Measure Information:
Title
Taste acceptability of ED
Description
Taste of at least one flavor of ED graded as 2 out of 5 by patient on nutritional diary taste acceptability scale (1=I really like the taste, 2=I like the taste, 3=The taste is acceptable, 4=I do not like the taste but can drink it, 5=I do not like the taste and cannot drink it).
Time Frame
Two weeks
Title
Change in incidence of vomiting
Description
No deterioration in incidence of vomiting as measured on MSAS scale. Grading 1 (occurring rarely) or 2 (occurring occasionally) is acceptable. Deterioration considered as change to 3 (occurring frequently) or 4 (occurring almost constantly).
Time Frame
Two weeks
Title
Change in incidence of pain
Description
No deterioration in incidence of abdominal pain as measured on MSAS scale. Grading 1 (occurring rarely) or 2 (occurring occasionally) is acceptable. Deterioration considered as change to 3 (occurring frequently) or 4 (occurring almost constantly).
Time Frame
Two weeks
Secondary Outcome Measure Information:
Title
The number of patients who can tolerate ED following presentation with IBO and can subsequently be treated with palliative chemotherapy
Description
Measured by reviewing hospital case notes
Time Frame
Two weeks
Title
Number of patients alive at the end of the study
Description
Measured by reviewing hospital case notes
Time Frame
Up to two years
Title
Health related quality of life
Description
Measured on EORTC-QLQ-C30
Time Frame
Two weeks
Title
Nutritional intake
Description
Measured by number of cartons taken by patient in 24 hours
Time Frame
Two weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age > 18 years Confirmed inoperable bowel obstruction due to disseminated malignancy Ability to tolerate 500ml of liquid Capacity to give informed consent Exclusion Criteria: Bowel obstruction that can be managed with surgical intervention Complete bowel obstruction and inability to tolerate small amount of liquid
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Eleanor Smith
Phone
01483 688547
Email
eleanor.smith@surrey.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Agnieszka Michael, MBBS PhD
Organizational Affiliation
Royal Surrey County Hospital, University of Surrey
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Surrey County Hospital NHS Foundation Trust
City
Guildford
State/Province
Surrey
ZIP/Postal Code
GU2 7XX
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Eleanor Smith
Phone
01483 688547
Email
eleanor.smith@surrey.ac.uk
First Name & Middle Initial & Last Name & Degree
Agnieszka Michael, MBBS PhD

12. IPD Sharing Statement

Plan to Share IPD
No

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EDMONd - Elemental Diet in Bowel Obstruction

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