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Sucrosomial Iron vs. Oral Iron Sulfate for the Treatment of Iron Deficiency Anemia in Patients With Ulcerative Colitis

Primary Purpose

Anemia, Iron Deficiency, Ulcerative Colitis

Status
Recruiting
Phase
Phase 3
Locations
Lebanon
Study Type
Interventional
Intervention
Sucrosomial Iron
Oral Iron
Sponsored by
American University of Beirut Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anemia, Iron Deficiency focused on measuring Sucrosomial Iron, Sideral Forte, Iron Supplementation, Iron Deficiency, Anemia, Ulcerative Colitis, Inflammatory Bowel Disease

Eligibility Criteria

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

Inclusion Criteria:

  • Age above 18
  • Confirmed diagnosis of Ulcerative Colitis
  • Proven Iron Deficiency Anemia (Hb < 12 for females and Hb < 13 for males AND iron saturation <20%)
  • Hemoglobin level > 8g/dl

Exclusion Criteria:

  • Age below 18
  • Hemoglobin level < 8g/dl
  • Recently hospitalized for disease flare (within 3 months)
  • Hemoglobinopathies (including thalassemia)
  • Isolated proctitis
  • Indeterminate colitis
  • Known liver or kidney disease
  • Known Celiac Disease
  • Extensive small bowel resection
  • Use of anticoagulants or aspirin
  • Known intolerance to oral iron therapy
  • Uninvestigated anemia
  • Pregnant or lactating women
  • Known hypersensitivity to iron sulfate
  • Transfusion in the past 4 weeks
  • Erythropoetin within the last 8 weeks
  • Rheumatoid Arthritis
  • History of menometrorrhagia or frequent epistaxis

Sites / Locations

  • American University of Beirut - Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sucrosomial Iron

Oral Iron Therapy

Arm Description

These patients will receive Sucrosomial Iron 30 mg + 70 mg ascorbic acid (Sideral Forte) twice daily

These patients will receive Oral Iron therapy at a dose of 195 mg twice daily for the same period of time

Outcomes

Primary Outcome Measures

Tolerability of experimental product
Tolerability will be assessed via a Treatment Tolerability Assessment Questionnaire

Secondary Outcome Measures

Response to iron repletion
Hemoglobin
Compliance and adherence
Regular Pill Counts
Response to iron repletion
Hematocrit
Response to iron repletion
Iron storage
Response to iron repletion
Iron saturation
Response to iron repletion
Ferritin

Full Information

First Posted
October 9, 2020
Last Updated
February 15, 2022
Sponsor
American University of Beirut Medical Center
Collaborators
Pharma M SAL, Lebanon
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1. Study Identification

Unique Protocol Identification Number
NCT05225545
Brief Title
Sucrosomial Iron vs. Oral Iron Sulfate for the Treatment of Iron Deficiency Anemia in Patients With Ulcerative Colitis
Official Title
Randomized Controlled Trial of Sucrosomial Iron vs. Oral Iron Sulfate for the Treatment of Iron Deficiency Anemia in Patients With Ulcerative Colitis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Recruiting
Study Start Date
November 4, 2019 (Actual)
Primary Completion Date
May 4, 2022 (Anticipated)
Study Completion Date
May 4, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
American University of Beirut Medical Center
Collaborators
Pharma M SAL, Lebanon

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 aim of the study is to compare the tolerability and efficacy of Sucrosomial Iron to Oral Iron Therapy in a randomized controlled trial for the treatment of Iron Deficiency Anemia in Ulcerative Colitis patients.
Detailed Description
Ulcerative Colitis (UC) is an inflammatory bowel disease (IBD) characterized by chronic inflammation limited to the mucosal layer of the colon. Anemia is a consistent clinical feature of IBD, and is encountered in one third of patients [1] and Anemia in Ulcerative Colitis is most commonly the result of iron-deficiency due to chronic blood loss through ulcerations in the colon. Oral Iron supplementation has been used for the treatment of Iron Deficiency anemia but may cause disease exacerbation in patients with UC [2]. Iron also can increase cancer risk [3], and is associated with many side effects such as constipation, diarrhea, nausea, vomiting, abdominal pain and hyperchromia of feces. Furthermore, studies have shown that oral iron supplementation fails to resolve anemia in 2 of 3 IBD patients. [4] Sucrosomial iron is a new preparation of iron pyrophosphate delivered within a phospholipid membrane and coated with sucrester (sucrose esters of fatty acids). it has been shown to have better absorption and higher bioavailability while minimizing side effects in multiple patient populations.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anemia, Iron Deficiency, Ulcerative Colitis
Keywords
Sucrosomial Iron, Sideral Forte, Iron Supplementation, Iron Deficiency, Anemia, Ulcerative Colitis, Inflammatory Bowel Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigator
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sucrosomial Iron
Arm Type
Experimental
Arm Description
These patients will receive Sucrosomial Iron 30 mg + 70 mg ascorbic acid (Sideral Forte) twice daily
Arm Title
Oral Iron Therapy
Arm Type
Active Comparator
Arm Description
These patients will receive Oral Iron therapy at a dose of 195 mg twice daily for the same period of time
Intervention Type
Drug
Intervention Name(s)
Sucrosomial Iron
Other Intervention Name(s)
Sideral Forte
Intervention Description
Experimental Arm
Intervention Type
Drug
Intervention Name(s)
Oral Iron
Intervention Description
Active Comparator
Primary Outcome Measure Information:
Title
Tolerability of experimental product
Description
Tolerability will be assessed via a Treatment Tolerability Assessment Questionnaire
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Response to iron repletion
Description
Hemoglobin
Time Frame
12 weeks
Title
Compliance and adherence
Description
Regular Pill Counts
Time Frame
12 weeks
Title
Response to iron repletion
Description
Hematocrit
Time Frame
12 weeks
Title
Response to iron repletion
Description
Iron storage
Time Frame
12 weeks
Title
Response to iron repletion
Description
Iron saturation
Time Frame
12 weeks
Title
Response to iron repletion
Description
Ferritin
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age above 18 Confirmed diagnosis of Ulcerative Colitis Proven Iron Deficiency Anemia (Hb < 12 for females and Hb < 13 for males AND iron saturation <20%) Hemoglobin level > 8g/dl Exclusion Criteria: Age below 18 Hemoglobin level < 8g/dl Recently hospitalized for disease flare (within 3 months) Hemoglobinopathies (including thalassemia) Isolated proctitis Indeterminate colitis Known liver or kidney disease Known Celiac Disease Extensive small bowel resection Use of anticoagulants or aspirin Known intolerance to oral iron therapy Uninvestigated anemia Pregnant or lactating women Known hypersensitivity to iron sulfate Transfusion in the past 4 weeks Erythropoetin within the last 8 weeks Rheumatoid Arthritis History of menometrorrhagia or frequent epistaxis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ali El Mokahal, MD
Phone
+961350000
Ext
5909
Email
ae136@aub.edu.lb
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ala Sharara, MD
Organizational Affiliation
American University of Beirut Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
American University of Beirut - Medical Center
City
Beirut
Country
Lebanon
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ala' I. Sharara, MD
Phone
009611350000
Ext
5345
Email
as08@aub.edu.lb
First Name & Middle Initial & Last Name & Degree
Ala' I Sharara, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
15247190
Citation
Gasche C, Lomer MC, Cavill I, Weiss G. Iron, anaemia, and inflammatory bowel diseases. Gut. 2004 Aug;53(8):1190-7. doi: 10.1136/gut.2003.035758.
Results Reference
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PubMed Identifier
12368409
Citation
Carrier J, Aghdassi E, Cullen J, Allard JP. Iron supplementation increases disease activity and vitamin E ameliorates the effect in rats with dextran sulfate sodium-induced colitis. J Nutr. 2002 Oct;132(10):3146-50. doi: 10.1093/jn/131.10.3146.
Results Reference
background
PubMed Identifier
12663492
Citation
Seril DN, Liao J, Yang GY, Yang CS. Oxidative stress and ulcerative colitis-associated carcinogenesis: studies in humans and animal models. Carcinogenesis. 2003 Mar;24(3):353-62. doi: 10.1093/carcin/24.3.353.
Results Reference
background
PubMed Identifier
24486177
Citation
Lugg S, Beal F, Nightingale P, Bhala N, Iqbal T. Iron treatment and inflammatory bowel disease: what happens in real practice? J Crohns Colitis. 2014 Aug;8(8):876-80. doi: 10.1016/j.crohns.2014.01.011. Epub 2014 Jan 31.
Results Reference
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Sucrosomial Iron vs. Oral Iron Sulfate for the Treatment of Iron Deficiency Anemia in Patients With Ulcerative Colitis

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