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Aphanizomenon Flos-aquae extract effect on mobilization of bone marrow stem cells

Effect of a Aphanizomenon Flos-aquae extract on mobilization of bone marrow stem cells and metabolic profile of patients with type 2 diabetes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201108074920N2
Enrollment
50
Registered
2013-07-19
Start date
2013-08-01
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

Type 2 Diabetes Mellitus. Diabetes Mellitus

Interventions

Intervention 1: Control group: 1 placebo capsule of StemFlo before breakfast and 2 placebo capsules of StemEnhance after dinner for a period of 12 weeks. Intervention 2: AFA (intervention) group: 1 c
Placebo
Treatment - Drugs
Control group: 1 placebo capsule of StemFlo before breakfast and 2 placebo capsules of StemEnhance after dinner for a period of 12 weeks
AFA (intervention) group: 1 capsule of StemFlo before breakfast and 2 capsules StemEnhance after dinner for a period of 12 weeks

Sponsors

Sabalan Talaee Asia Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with type 2 diabetes; between 20 to 60 years with HbA1C=7.5% will be included in the study. Exclusion criteria are pregnancy; presence advanced diabetic complications; renal failure or cardiovascular disease; use of vitamin or mineral supplements in the last 2 months before the study; change or introduction of new medications to the treatment of diabetes, and a history of inflammatory illness or cancer.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stem cell marker of CD34. Timepoint: Before and After treatment (0 and 12 weeks). Method of measurement: Flocytometry method.

Secondary

MeasureTime frame
Blood Urea Nitrogen (BUN). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;C-peptide. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;Low Density Lipoprotein (LDL). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;Interleukine-6 (IL-6). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;Malon Dialdehyde (MDA). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;SGOT. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;SGPT. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;TNF-a. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;Total Cholestrol. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;Triglyceride. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;Fasting Blood Sugar. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;Creatinine. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Elisa.;High Density Lipoprotein (HDL). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Enzymatic Calorimetry.;Glycosylated Hemoglobin (HbA1c). Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Chromatography.;Height. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Stadiometer.;Weight. Timepoint: Before and After Treatment (0 and 12 weeks). Method of measurement: Digital weight gauge.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Sanaei

Chronic Diseases Research Center

sanaeimaryam@yahoo.com+98 21 8835 4158

Outcome results

None listed

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