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Laxative Properties of Microencapsulated Lipid (Constipation Study)

Primary Purpose

Constipation

Status
Recruiting
Phase
Not Applicable
Locations
Ireland
Study Type
Interventional
Intervention
Fat Microcapsules
Sponsored by
University College Dublin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Constipation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18-65 years
  • Engaged in weight loss treatment
  • Diagnosis of chronic constipation (Rome IV criteria)1
  • Capacity to consent to participate

Exclusion Criteria:

  • Substance abuse
  • Pregnancy
  • Patients who are taking medication for constipation should be on stable doses of medications for constipation for more than 2 weeks. They should neither start nor stop any medication for constipation in the 2 weeks prior to the visits.

Sites / Locations

  • Clinical Research CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Microencapsulated fat stomach

Microencapsulated fat intestine

Arm Description

Participants will consume a drink containing 400kcal of microencapsulated fat that will be released in the stomach.

Participants will consume a drink containing 400kcal of microencapsulated fat that will be released in the intestine.

Outcomes

Primary Outcome Measures

Completed bowel motion
Proportion of participants reporting a completed bowel motion within 24 hours.

Secondary Outcome Measures

Hunger
Hunger scores as measured by Visual Analogue Scales, the scale has a score from 0 to 100 with 0 being least hungry and 100 being most hungry.
calories
Number of calories consumed during an ad libitum meal
Gut hormones
Gut hormones concentration
Fullness
Fullness scores as measured by Visual Analogue Scales, the scale has a score from 0 to 100 with 0 being least full and 100 being most full

Full Information

First Posted
April 4, 2022
Last Updated
May 25, 2022
Sponsor
University College Dublin
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1. Study Identification

Unique Protocol Identification Number
NCT05324241
Brief Title
Laxative Properties of Microencapsulated Lipid (Constipation Study)
Official Title
A Proof of Principle Study of the Laxative Properties of Microencapsulated Lipid in Patients Experiencing Constipation Related to Intentional Weight Loss
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
April 15, 2022 (Actual)
Primary Completion Date
April 15, 2023 (Anticipated)
Study Completion Date
April 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College Dublin

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
The present study seeks to build on these observations to assess whether in principle, fat containing microcapsules might help patients experiencing constipation in association with weight loss interventions (including GLP-1 analogues or bariatric surgery) to both avoid/treat constipation and simultaneously optimise their ability to feel full during eating. This potential dual action may provide added benefit versus the use of traditional approaches to constipation prophylaxis e.g., lactulose.
Detailed Description
Chronic constipation most frequently arises as a functional disorder of at least 3 months duration, the aetiology of which is multifactorial encompassing dietary and lifestyle factors arising in the context of intact colonic motility. Confirmatory clinical diagnosis of chronic constipation under this definition can be made with reference to the Rome IV criteria encompassing assessment of stool frequency, quality, straining etc. Whilst broadly prevalent across the population, constipation is particularly troublesome in a significant number of patients undergoing interventions for weight loss in obesity, be that dietary, pharmacological or surgical. Calorie restriction per se, which is a common feature of most interventions for obesity necessarily reduces stimulation of colonic motility by impacting the frequency and intensity of colonic mass movements. Moreover, decreases in dietary fibre during food restriction result in debulking of the stool. Multiple dietary and pharmacological approaches to the management of chronic constipation are available to mitigate the risk of constipation during weight loss and treat it when it becomes manifest. However, these can often be poorly accepted due to gastrointestinal side effects. Interestingly, the potential laxative properties of orlistat, a pancreatic lipase inhibitor-based treatment for morbid obesity have been investigated in off-label studies in the setting of idiopathic chronic constipation and constipation associated with opioid pain medication and anti-psychotic (clozapine) therapy. Mechanism of action in these cases most probably relates to the pro-kinetic and lubricatory effects of the increasing passage of undigested fat to the colon. Based on these case series, the potential for weight loss pharmacotherapy with in-built mitigation of associated constipation becomes an attractive concept. When digestive and absorptive processes are impeded or moved distally in the small intestine, as can happen with respect to dietary triglycerides during orlistat therapy, satiety gut hormone signal and quantity of food intake are affected. During an ileal infusion of a lipid emulsion, healthy subjects ate a smaller amount compared to control infusions. A study in healthy volunteers in which fat was delivered via a nasal tube to the duodenum, jejunum and ileum found that the ileal treatment had the most pronounced effect on food intake and satiety. The investigators have used a new food encapsulation technology using natural food grade pea protein, AnaBio©*, to deliver pure oleic acid to the distal small intestine showed significant attenuation of food intake in association with enhancement of enteroendocrine satiety hormone release. The results recorded an increase in the number of bowel motions over the subsequent 24 hours in half of the participants. Subsequently, the investigators showed that ingestion of a smaller 400kcal cargo of microencapsulated oleic acid resulted in decreased hunger and food intake, no increase in the frequency of bowel motion but an increase in stool softness. Based on the above data the investigators are encouraged to proceed with the present study, the main goal of which is therefore to investigate whether the 400kcal dose of encapsulated fat delivered to the distal small intestine might be a useful supportive therapy in patients engaged in intensive weight loss therapies and experiencing constipation as a consequence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Constipation

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
31 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Microencapsulated fat stomach
Arm Type
Experimental
Arm Description
Participants will consume a drink containing 400kcal of microencapsulated fat that will be released in the stomach.
Arm Title
Microencapsulated fat intestine
Arm Type
Experimental
Arm Description
Participants will consume a drink containing 400kcal of microencapsulated fat that will be released in the intestine.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fat Microcapsules
Intervention Description
Consumption of a drink that contains microencapsulated fat that will be released either in the stomach or in the distal small intestines.
Primary Outcome Measure Information:
Title
Completed bowel motion
Description
Proportion of participants reporting a completed bowel motion within 24 hours.
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Hunger
Description
Hunger scores as measured by Visual Analogue Scales, the scale has a score from 0 to 100 with 0 being least hungry and 100 being most hungry.
Time Frame
6 hours
Title
calories
Description
Number of calories consumed during an ad libitum meal
Time Frame
6 hours
Title
Gut hormones
Description
Gut hormones concentration
Time Frame
6 hours
Title
Fullness
Description
Fullness scores as measured by Visual Analogue Scales, the scale has a score from 0 to 100 with 0 being least full and 100 being most full
Time Frame
6 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18-65 years Engaged in weight loss treatment Diagnosis of chronic constipation (Rome IV criteria)1 Capacity to consent to participate Exclusion Criteria: Substance abuse Pregnancy Patients who are taking medication for constipation should be on stable doses of medications for constipation for more than 2 weeks. They should neither start nor stop any medication for constipation in the 2 weeks prior to the visits.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carel le Roux
Phone
+353864117842
Email
carel.leroux@ucd.ie
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carel le Roux
Organizational Affiliation
University College Dublin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinical Research Centre
City
Dublin
ZIP/Postal Code
Dublin 4
Country
Ireland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carel le Roux
Phone
+353864117842
Email
carel.leroux@ucd.ie

12. IPD Sharing Statement

Plan to Share IPD
No

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Laxative Properties of Microencapsulated Lipid (Constipation Study)

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