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Main
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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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PACTR |
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Last refreshed on:
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29 April 2013 |
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Main ID: |
PACTR201111000337258 |
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Date of registration:
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10/11/2011 |
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Primary sponsor: |
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Public title:
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Clinical validation of Grewia tenax fruits extract chewble tablets in treatment of iron deficiency anemia [retrospectively registered]
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Scientific title:
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Randomized control trial to validate Grewi tenax fruits extract chewable tablets in the treatment of iron deficiency anemia in adults. A pilot study |
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Date of first enrolment:
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2011-08-15 |
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Target sample size:
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70 |
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Recruitment status: |
Open to recruitment: actively recruiting participa |
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URL:
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HTTP://www.pactr.org/ATMWeb/appmanager/atm/atmregistry?da=true&tno=PACTR201111000337258 |
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Study type:
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interventional |
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Study design:
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Parallel: different groups receive different interventions at same time during study,
Randomised,
By tossing a coin to allocate subjects ,
simple randomization by tossing a coin,
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Countries of recruitment
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South Africa
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Contacts
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Name:
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Sami
Khalid |
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Address:
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AlNus street
11111
Khartoum
Sudan |
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Telephone:
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00249912146087 |
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Email:
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khalidseek@hotmail.com |
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Affiliation:
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Scientific Supervisor |
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Name:
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Randa
AlMahdi |
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Address:
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P O Box 11580
11111
Khartoum
Sudan |
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Telephone:
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00249912147698 |
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Email:
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randa_almahdi@yahoo.com |
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Affiliation:
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primary investigator |
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Key inclusion & exclusion criteria
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Inclusion criteria: Inclusion criteria: Volunteer adults 18 years and older diagnosed and confirmed to have iron deficiency whose hemoglobin measurements are 78% g/dl or less who may or may not have iron deficiency symptoms to be recruited after signing an informed consent.
Exclusion criteria: Exclusion Criteria:
Other types of anemias other than iron deficiency
GIT disorders that may interfere with oral absorption
All hemoglobinopathies and blood disorders
Other comorbidities that may confound the results outcome as seen by the supervising physicians
Age minimum:
18 Year
Age maximum:
65 Year
Gender:
Female
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Health Condition(s) or Problem(s) studied
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iron deficiency and iron deficiency anemia
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Primary Outcome(s)
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Hemoglobin level, reticulocyte count and full iron profile
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Secondary Outcome(s)
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Reported adverse effects with each treatment arm and clinical improvement of anemia
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Source(s) of Monetary Support
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Privately by the researcher: Randa AlSadig AlMahdi
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