Effect of the Consumption of Ferric Hydroxide Adipate on Urinary Phosphorus Excretion.
Primary Purpose
Healthy, Chronic Kidney Diseases
Status
Completed
Phase
Early Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Calcium acetate
Iron Hydroxide Adipate
Placebo
Sponsored by
About this trial
This is an interventional basic science trial for Healthy focused on measuring urinary phosphate, iron hydroxide, hypophosphatemia, phosphate binder, ferric hydroxide adipate
Eligibility Criteria
Inclusion Criteria:
- Males and females, aged >18 years, who are generally healthy.
Exclusion Criteria:
- Pregnancy and lactation
- iron deficiency and iron deficiency anaemia
- weight change of +/-2kg in the past month
- dysphagia
- surgery in the past three months
- cancer in the last ten years
- diabetes
- known medical and genetic conditions interfering with calcium and phosphate metabolism: e.g. hyper/hypo-parathyroidism, Fanconi syndrome, hyper/hypothyroidism (except individuals who are taking stable doses of thyroid hormones)
- chronic infection or chronic inflammation
- cardiovascular disease
- chronic respiratory disease
- abnormal renal function (based on glomerular filtration rate)
- known renal disease
- abnormal liver function/known liver disease
- hereditary haemochromatosis or haemoglobinopathies
- gastrointestinal disease
- bone disease
- hypertension
- current use of proton pump inhibitors
- use of other medication that affects mineral homeostasis (on a case by case basis, in consultation with HNR clinician)
- Extreme muscle hypertrophy (e.g. body building)
Sites / Locations
- MRC Human Nutrition Research
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Placebo Comparator
Active Comparator
Experimental
Arm Label
Methylcellulose
Calcium Acetate
Iron Hydroxide Adipate
Arm Description
On one of the study days: ingest one methylcellulose capsule with a test meal rich in phosphate.
On one of the study days: ingest 667 mg calcium acetate, equivalent to 169 mg elemental calcium, with a test meal rich in phosphate.
On one of the study days: ingest 800 mg ferric hydroxide adipate, equivalent to 175 mg elemental iron, with a test meal rich in phosphate.
Outcomes
Primary Outcome Measures
urinary phosphate
To determine if the ingestion of ferric hydroxide adipate with food induces a reduction in urinary phosphate concentration, compared with the administration of placebo plus the same food on a different occasion.
Secondary Outcome Measures
iron absorption
iron absorption from the ferric hydroxide adipate treatment will be determined by labelling this preparation with 58Fe and measuring day 14 erythrocyte 57Fe:58Fe.
Full Information
NCT ID
NCT01991574
First Posted
November 18, 2013
Last Updated
February 3, 2017
Sponsor
Medical Research Council
1. Study Identification
Unique Protocol Identification Number
NCT01991574
Brief Title
Effect of the Consumption of Ferric Hydroxide Adipate on Urinary Phosphorus Excretion.
Official Title
Study of the Effect of the Consumption of Ferric Hydroxide Adipate on Urinary Phosphorus.
Study Type
Interventional
2. Study Status
Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
October 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical Research Council
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Ferric hydroxide adipate is a ferric iron supplement containing iron hydroxide and a dietary organic acid that was developed at MRC Human Nutrition Research. We aim to determine if the ingestion of ferric hydroxide adipate with food induces a reduction in urinary phosphate concentration, compared with the administration of placebo plus the same food on a different occasion. We hypothesise that ferric hydroxide adipate binds some phosphate ions in the gastrointestinal tract, which prevents part of the phosphate load in a meal from being absorbed. On another visit, calcium will be given with the same food, as a positive control, since this element is well known to restrict dietary phosphate absorption through the formation of insoluble calcium phosphates in the gut lumen. We will compare urinary phosphate concentrations after co-ingestion of the calcium salt and food versus urinary phosphate following ferric hydroxide adipate and the same food. Additionally, the calcium data will be compared with placebo data, since a significant reduction in urinary phosphate concentrations after calcium treatment will confirm the suitability of the study design.
Finally, iron absorption from the ferric hydroxide adipate treatment will be determined by labelling this preparation with 58Fe and measuring day 14 erythrocyte 57Fe:58Fe.
The study design is: Three-way cross-over volunteer absorption study. Volunteers will not be told which treatment they receive (placebo, ferric hydroxide adipate, or supplemental calcium). Researchers co-ordinating the study on a day to day basis will be aware of treatment allocation, but analysts will not be told which samples correspond to which treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Healthy, Chronic Kidney Diseases
Keywords
urinary phosphate, iron hydroxide, hypophosphatemia, phosphate binder, ferric hydroxide adipate
7. Study Design
Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Methylcellulose
Arm Type
Placebo Comparator
Arm Description
On one of the study days: ingest one methylcellulose capsule with a test meal rich in phosphate.
Arm Title
Calcium Acetate
Arm Type
Active Comparator
Arm Description
On one of the study days: ingest 667 mg calcium acetate, equivalent to 169 mg elemental calcium, with a test meal rich in phosphate.
Arm Title
Iron Hydroxide Adipate
Arm Type
Experimental
Arm Description
On one of the study days: ingest 800 mg ferric hydroxide adipate, equivalent to 175 mg elemental iron, with a test meal rich in phosphate.
Intervention Type
Drug
Intervention Name(s)
Calcium acetate
Intervention Type
Dietary Supplement
Intervention Name(s)
Iron Hydroxide Adipate
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
methylcellulose capsules
Primary Outcome Measure Information:
Title
urinary phosphate
Description
To determine if the ingestion of ferric hydroxide adipate with food induces a reduction in urinary phosphate concentration, compared with the administration of placebo plus the same food on a different occasion.
Time Frame
9 hours
Secondary Outcome Measure Information:
Title
iron absorption
Description
iron absorption from the ferric hydroxide adipate treatment will be determined by labelling this preparation with 58Fe and measuring day 14 erythrocyte 57Fe:58Fe.
Time Frame
14 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
- Males and females, aged >18 years, who are generally healthy.
Exclusion Criteria:
Pregnancy and lactation
iron deficiency and iron deficiency anaemia
weight change of +/-2kg in the past month
dysphagia
surgery in the past three months
cancer in the last ten years
diabetes
known medical and genetic conditions interfering with calcium and phosphate metabolism: e.g. hyper/hypo-parathyroidism, Fanconi syndrome, hyper/hypothyroidism (except individuals who are taking stable doses of thyroid hormones)
chronic infection or chronic inflammation
cardiovascular disease
chronic respiratory disease
abnormal renal function (based on glomerular filtration rate)
known renal disease
abnormal liver function/known liver disease
hereditary haemochromatosis or haemoglobinopathies
gastrointestinal disease
bone disease
hypertension
current use of proton pump inhibitors
use of other medication that affects mineral homeostasis (on a case by case basis, in consultation with HNR clinician)
Extreme muscle hypertrophy (e.g. body building)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jonathan Powell, PhD
Organizational Affiliation
Medical Research Council
Official's Role
Study Chair
Facility Information:
Facility Name
MRC Human Nutrition Research
City
Cambridge
State/Province
Cambridgeshire
ZIP/Postal Code
CB1 9NL
Country
United Kingdom
12. IPD Sharing Statement
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Effect of the Consumption of Ferric Hydroxide Adipate on Urinary Phosphorus Excretion.
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