Last updated: 11/03/2018 16:21:16
A study to demonstrate the efficacy and tolerability of ferrous bisglycinate chelate in iron deficiency anaemia and to compare these with those of ferrous ascorbate.
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A multicentre, randomized, laboratory-blinded, parallel-group study to demonstrate the efficacy and tolerability of ferrous bisglycinate chelate in iron deficiency anaemia and to compare these with those of ferrous ascorbate.
Trial description: Iron deficiency anaemia (Haemoglobin, Hb < 12gm/dl) is one of India’s major public health problems particularly in women. Effective control of iron deficiency anaemia decreases the incidence of fatigue, bodyache, headache, lack of concentration and menstrual complications. Iron bisglycine chelate has been used successfully to treat iron deficiency anaemia and is also a well tolerated therapy. Use of ferrous bisglycinate chelate one tablet daily as a nutritional supplement is well established in India. For treatment of iron deficiency anaemia, some women may need 1 tablet/day, while some may need 2 tablets/day. In India, ferrous ascorbate, 1 tablet daily is a widely accepted form of treatment for iron deficiency anaemia. The primary purpose of this study is to demonstrate the efficacy and tolerability profile of ferrous bisglycinate chelate to support the registration of this product as a ‘drug’ in India. Comparative data between ferrous bisglycinate chelate and ferrous ascorbate will also augment our existing knowledge, which will further support appropriate use of ferrous bisglycinate chelate for the treatment of iron deficiency anaemia. Study design and patient population: This will be a multicentre, randomized, laboratory-blinded, parallel- group study. It is projected that the study will randomize 270 women (90 subjects in each treatment arm) with iron deficiency anaemia (Hb 6-9 gm/dl + serum Ferritin <15 μg/l) to either ferrous bisglycinate chelate 1 or 2 tablets/day, or ferrous ascorbate 1 tablet/day for 8 weeks. At fortnightly visits, blood will be collected for Hb (to evaluate efficacy), adverse events will be documented (to evaluate tolerability), the investigational drugs will be dispensed and reasons for non compliance will be recorded. Study endpoints: The primary endpoint is defined as the rise of Hb from baseline after 8 weeks of treatment in each ferrous bisglycinate chelate group (1 tablet/day and 2 tablets/day). The secondary endpoints include the difference in the average change in Hb, difference in the rate of rise of Hb, difference in the proportion of patients who achieve a target Hb ≥12gm/dl and difference in the % incidence of gastrointestinal side effects during 8 week therapy with 2 dosing regimens of ferrous bisglycinate chelate (1 tablet/day and 2 tablets/day) and ferrous ascorbate 1 tablet/day.
Primary purpose:
Other
Trial design:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:
Change from Baseline in hemoglobin (Hb) after 8 weeks of treatment in each ferrous bisglycinate chelate group (1 tablet daily and 2 tablets daily)
Timeframe: Baseline and Week 8
Secondary outcomes:
Mean change in Hb from Baseline to 8 weeks
Timeframe: Baseline to Week 8
Percentage of participants who achieved a target Hb more than or equal to 12 gm/dL after 8 weeks of treatment
Timeframe: Up to Week 8
Mean change in Hb during 8 weeks therapy
Timeframe: Up to Week 8
Difference in percentage of participants with gastrointestinal side effects during 8 weeks treatment with ferrous bisglycinate chelate and ferrous ascorbate
Timeframe: Up to Week 8
Interventions:
Enrollment:
271
Primary completion date:
2011-18-02
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Haematopoiesis
Product
GSK2594163
Collaborators
Not applicable
Study date(s)
October 2010 to February 2011
Type
Interventional
Phase
3
Participation criteria
Sex
Female
Age
18 - 55 years
Accepts healthy volunteers
No
- Inclusion Criteria
- Subjects eligible for enrolment to the study must meet all of the following criteria:
Inclusion and exclusion criteria
Inclusion criteria:
- Inclusion Criteria Subjects eligible for enrolment to the study must meet all of the following criteria: 1.Signed and dated written informed consent is obtained prior to participation. 2.Female outpatients between 18 to 55 years of age and using effective method of contraception if sexually active. 3.Non use of any iron supplement for 3 months prior to enrolment to the study. 4.Presence of iron deficiency anaemia: low haemoglobin (Hb 6-9 gm/dl) + low serum ferritin (<15 μg/l). 5.No occult blood in stool. 6.Able to comply with the requirements of the protocol. 7.Subjects should have a valid telephone contact. Exclusion Criteria Subjects meeting any of the following criteria must not be enrolled to the study: 1.Pregnancy (confirmed by urine dipstick method) 2.Desire to conceive within the next 3 months including patients who are receiving treatment to facilitate conception. 3.Lactating women. 4.Medical history of current hematological disorders other than iron deficiency anaemia (e.g. aplastic anaemia, megaloblastic anaemia, sideroblastic anaemia, pernicious anaemia, thalassemia, sickle cell anaemia, etc.). 5.Medical history of thyroid dysfunction. 6.Medical history of chronic renal disease. 7.Medical history of malabsorption syndrome, haemochromatosis and haemosiderosis, hypochlorhydria, achlorhydria, gastrectomy, gastrojejunostomy. 8.Inability to withhold prohibited medication. 9.Obvious internal or external bleeding as documented by medical history and/or examination if considered clinically significant in the opinion of the investigator. 10.Clinically significant abnormality in laboratory reports and/or ECG. 11.Medical history of hepatitis B, hepatitis C and/or exposure to HIV. 12.Serious, uncontrolled disease (other than thyroid dysfunction and chronic renal disease) including serious psychological disorders likely to interfere with the study and/or likely to cause death within the study period. 13.Participation in another clinical trial in the last 8 weeks before entry to Visit 0. 14.Evidence of alcohol or drug abuse, that may, in the opinion of the investigator interfere with study compliance or prevent understanding of the objectives, investigational procedures or possible consequences of the study. 15.Known or suspected hypersensitivity to iron or any of the components of ferrous bisglycinate chelate or ferrous ascorbate tablets.
Trial location(s)
Showing 1 - 6 of 7 Results
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2011-18-02
Actual study completion date
2011-18-02
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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