Impact of Mulberry Leaf on Type 2 Diabetes (Mul-DM)
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ClinicalTrials.gov Identifier: NCT00795704 |
Recruitment Status :
Completed
First Posted : November 21, 2008
Results First Posted : August 9, 2012
Last Update Posted : August 9, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Type 2 Diabetes | Drug: Mulberry Leaf Extract Drug: Placebo | Phase 2 Phase 3 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 24 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Effect of Mulberry Leaf Extract on Glycemic Durability in Non-insulin Dependent Diabetes Mellitus: a Double-blind, Randomized, Placebo-controlled Pilot Study (Mul-DM) |
Study Start Date : | April 2008 |
Actual Primary Completion Date : | May 2010 |
Actual Study Completion Date : | May 2010 |

Arm | Intervention/treatment |
---|---|
Placebo Comparator: Placebo
Control Group
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Drug: Placebo
Placebo 500 mg #2 capsules by mouth three times daily |
Active Comparator: Mulberry Leaf Extract |
Drug: Mulberry Leaf Extract
Mulberry Leaf Extract 1000 mg by mouth three times daily for 3 months
Other Names:
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- Hemoglobin A1C [ Time Frame: 3 month minus baseline ]
- Number of Participants With Adverse Drug Reactions, Abnormal Metabolic Panel Levels, or Abnormal Liver Enzyme Levels [ Time Frame: Baseline, 1 month, and 3 months ]Sodium (>150 mmol/L), Potassium (>5 mmol/L), Bicarbonate (>34 mmol/L), Chloride (>110 mmol/L), Serum Creatinine (>1.2 mg/dL), Blood Urea Nitrogen (24 mg/dL), Calcium (>11 mg/L), Alanine Aminotransferase (>3 times baseline), Aspartate Aminotransferase (>3 times baseline) were collected at baseline, 1 month, and 3 months. Self-Reported adverse drug reactions are also reported.
- Change From Baseline in Self-Monitoring Blood Glucose (SMBG) Averages [ Time Frame: Baseline and 3 months ]2-hour postprandial SMBG reported. A negative value indicates a decrease from baseline. A positive value indicates an increase from baseline.

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Type 2 diabetes
- No diabetes medication adjustments for at least 2 months
- Stable hemoglobin A1C [Between 7.0% to 8.0% (inclusive) and not varying by more than 10% since prior visit; If no A1C exists prior to the current visit and no medication adjustments are made, the current A1C may used as the baseline]
Exclusion Criteria:
- On insulin
- History of overt cardiovascular disease
- History of missed appointments or non-compliance with medications
- History of hepatic or renal insufficiency
- History of hemoglobinopathies
- Women of reproductive potential not on oral contraceptives
- Pregnant/nursing women.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00795704
United States, Mississippi | |
University of Mississippi Medical Center | |
Jackson, Mississippi, United States, 39216 |
Principal Investigator: | Daniel M Riche, Pharm.D. | University of Mississippi Medical Center |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Daniel Riche, Assistant Professor of Pharmacy Practice and Medicine, University of Mississippi Medical Center |
ClinicalTrials.gov Identifier: | NCT00795704 |
Other Study ID Numbers: |
2008-0053 |
First Posted: | November 21, 2008 Key Record Dates |
Results First Posted: | August 9, 2012 |
Last Update Posted: | August 9, 2012 |
Last Verified: | June 2012 |
Herbal Supplement Type 2 Diabetes Mulberry Hemoglobin A1C |
Diabetes Mellitus Diabetes Mellitus, Type 2 Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases |