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The effect of Medicago Sativa syrup on the platelet count of patients with Idiopathic Thrombocytopenic Purpura

The effect of Medicago Sativa syrup on the platelet count of patients with ITP (Idiopathic Thrombocytopenic Purpura)

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017010924993N2
Enrollment
40
Registered
2017-02-04
Start date
2017-02-03
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Thrombocytopenic Purpura. Idiopathic Thrombocytopenic Purpura

Interventions

Intervention 1: In the intervention group, Medicago Sativa syrup containing 650 mg of extract of alfalfa in each 5 ml and daily intake of patients is 5 ml every eight hours. Intervention 2: The contro
Treatment - Drugs
In the intervention group, Medicago Sativa syrup containing 650 mg of extract of alfalfa in each 5 ml and daily intake of patients is 5 ml every eight hours.
The control group will be received 5 ml placebo syrup is administered every eight hours.

Sponsors

Research and Technology Vice-Chancellory of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the definitive diagnosis of ITP resistant to corticosteroids or corticosteroid dependent by an expert hematologist; platelet count between 50,000 to 150,000; aged between 15 and 50 years; lack of spontaneous bleeding; lack of other blood diseases; lack of systemic disease such as lupus erythematosus; lack of pregnancy; desire to attend the project Exclusion criteria: an active and spontaneous bleeding; need to hospitalization; thrombocytopenia below 50,000; infectious disease; pregnancy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Platelet count. Timepoint: Baseline, the end of the study. Method of measurement: Laboratory blood test.

Secondary

MeasureTime frame
Complete Blood Count. Timepoint: Baseline, the end of the study. Method of measurement: Laboratory blood test.;Bleeding Time. Timepoint: Baseline, the end of the study. Method of measurement: Laboratory blood test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamideh Naghedi Baghdar

Faculty of Iranian Traditional Medicine of Mashhad University of Medical Sciences

tim@mums.ac.ir; naghedih911@mums.ac.ir+98 51 3855 2188

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026