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Clinical Evaluation of the Pharmacokinetic Goldenseal-Metformin Interaction in Diabetic Patients

Clinical Evaluation of the Pharmacokinetic Goldenseal-Metformin Interaction in Diabetic Patients

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05081583
Enrollment
22
Registered
2021-10-18
Start date
2021-09-16
Completion date
2023-08-31
Last updated
2024-12-19

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

Conditions

Diabetes Mellitus, Type 2, Interaction, Adverse Herb-Drug

Keywords

pharmacokinetics, natural product-drug interactions, transporters

Brief summary

Supplements containing goldenseal, a perennial herb native to North America, have consistently ranked among the top 20 highest selling natural products throughout the last decade. Goldenseal products are marketed as licensed natural health products in Canada and as dietary supplements in the United States. Natural products made from dried roots of the goldenseal plant are purported to have therapeutic value and are used to self-treat a range of medical complications, including the common cold, allergic rhinitis, and digestive disorders, such as diarrhea and constipation. Based on a previous clinical study, goldenseal have been shown to precipitate pharmacokinetic interactions with metformin in healthy volunteers. This follow-up study aims to evaluate the goldenseal-metformin interaction in type 2 diabetic patients. Results from this proposed clinical study will (1) characterize the pharmacokinetic interaction between the botanical dietary supplement goldenseal and anti-diabetic drug metformin, (2) provide evidence-based recommendations to mitigate drug interaction risks, and (3) contribute to the development of a comprehensive strategy for effectively assessing other potential natural-product drug interactions.

Detailed description

Many patient groups, including those afflicted with cardiovascular disease, cancer, HIV/AIDS, hepatitis C, and diabetes, often supplement their prescribed pharmacotherapeutic regimens with herbal and other natural products, raising concern for adverse interactions. Unlike for drug-drug interactions, rigorous, harmonized guidelines for assessing the risk of natural product-drug interactions do not exist. The NCCIH-funded Center of Excellence for Natural Product Drug Interaction (NaPDI) Research was established in September 2015. The mission of the NaPDI Center is to provide leadership in the identification, evaluation, and dissemination of potential clinically meaningful pharmacokinetic natural product-drug interactions. Goldenseal is one of four high priority natural products selected by the NaPDI Center for further evaluation for drug interaction potential. A recent clinical study completed by researchers at the NaPDI center showed that a well-characterized, adulterant- and contaminant-free goldenseal product administered to 16 healthy volunteers (3 g daily by mouth for 6 consecutive days) resulted in a significant decrease (23%) in metformin systemic exposure \[area under the plasma concentration-time curve (AUC)\] with no change in half-life or renal clearance. Based on these clinical observations, along with complementary in vitro data, the current working hypothesis is that goldenseal interacts with intestinal organic cation transporter 1 to alter metformin disposition. These observations may have clinical implications for diabetic patients, as metformin is the first-line treatment and most prescribed anti-diabetic medication for type 2 diabetes. The objective of this study is to assess the potential for goldenseal to alter the pharmacokinetics and clinical effects of standard metformin treatment in well-controlled adult type 2 diabetic patients. Transporter inhibition represents an understudied mechanism of natural product-drug interactions. The proposed clinical study will be the first of its kind to evaluate whether such pharmacokinetic interactions can potentially affect clinical outcomes. The knowledge gained from these efforts will ultimately build upon a systematic framework for effectively studying other transporter-mediated natural product-drug interactions.

Interventions

DRUGMidazolam Hcl 1Mg/Ml Inj

0.5 mL of an intravenous solution (1 mg/mL) will be administered.

DIETARY_SUPPLEMENTGoldenseal (Hydrastis canadensis)

Goldenseal (Solaray; Lot #1020199) is supplied as dried root powder in vegetable capsules, each containing 550 mg of herbal content. Goldenseal capsules will be administered with 240 mL of water.

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
Washington State University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* are 18-65 years old and healthy * have been medically diagnosed with Type 2 diabetes and currently taking metformin (1- 2 g daily), but otherwise healthy as determined by the study physician * have an HbA1c \< 8% as determined by laboratory analysis on initial screening * are not taking any medications, dietary/herbal supplements, or citrus juices that can interfere with your ability to eliminate the study drugs and goldenseal from your body * are willing to stop consuming alcohol, caffeinated beverages or other caffeine- containing products the evening before and the morning of the first day of each study arm * are female and are willing to use an acceptable method of birth control that does not include oral birth control pills or patches (such as abstinence, copper IUD, condom) * can provide written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for the subject to comply with the requirements of the study

Exclusion criteria

* have an HbA1c ≥ 8% * have other chronic illnesses other than type 2 diabetes (e.g., type 1 diabetes, kidney disease, hepatic disease, uncontrolled hypertension, coronary artery disease, chronic obstructive pulmonary disease, cancer, or HIV/AIDS) * have a hematologic (blood) disorder * have a history of drug or alcohol abuse * have any major psychiatric illness * are pregnant or breastfeeding * have a history of intolerance or allergy to midazolam or goldenseal products * are taking concomitant medications, both prescription and non-prescription (including dietary supplements/herbal products) known to alter the pharmacokinetics of either study drug or goldenseal constituents

Design outcomes

Primary

MeasureTime frameDescription
Metformin AUCBefore and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.Area under the plasma concentration time curve of metformin
Metformin CmaxBefore and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.maximum concentration of metformin

Secondary

MeasureTime frameDescription
Midazolam AUCBefore and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.area under the concentration vs. time curve of midazolam
Metformin Half-Life0-24hhalf-life of metformin
Metformin Renal Clearance0-24hrenal clearance of metformin

Countries

United States

Participant flow

Pre-assignment details

A washout period of ≥7 days between each arm was implemented in the study design.

Participants by arm

ArmCount
Midazolam Alone - Washout - Midazolam + Acute Goldenseal - Washout - Midazolam + Chronic Goldenseal
Twenty-two adults (12 males, 10 females) with type 2 diabetes participated in this three-arm, crossover study to assess a pharmacokinetic natural product-drug interaction. In arm 1 (midazolam alone), participants were administered a single dose of midazolam (0.5 mg) intravenously via a peripherally inserted catheter; at this time, participants were instructed to co-administer their entire daily dose of metformin orally. For Arm 2 (midazolam + acute goldenseal exposure), the same 22 participants were administered a single dose of goldenseal (3.3 g) orally 30 minutes prior to administration of midazolam and metformin. For Arm 3 (chronic goldenseal exposure), participants self-administered goldenseal (1.1 g) orally three times daily for 27 days. On the 28th day, participants were administered the goldenseal three times daily, as well as the single dose of midazolam and metformin. Plasma and urine were collected from 0-24 hours post-midazolam administration for all 3 arms of the study. A washout period of 7 days separated each arm to ensure appropriate washout of midazolam. Participants continued their routine administration of metformin as prescribed throughout the duration of the study without interruption in pharmacotherapy. Midazolam HCl 1mg/mL inj: 0.5 mL of intravenous solution Goldenseal (Hydrastis canadensis) 550 mg capsules: dried root powder in vegetable capsules (Solaray; Lot #1020199)
22
Total22

Baseline characteristics

CharacteristicMidazolam Alone - Washout - Midazolam + Acute Goldenseal - Washout - Midazolam + Chronic Goldenseal
Age, Categorical
<=18 years
0 Participants
Age, Categorical
>=65 years
0 Participants
Age, Categorical
Between 18 and 65 years
22 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
2 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
17 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
3 Participants
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants
Race (NIH/OMB)
Asian
0 Participants
Race (NIH/OMB)
Black or African American
0 Participants
Race (NIH/OMB)
More than one race
1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants
Race (NIH/OMB)
White
20 Participants
Sex: Female, Male
Female
10 Participants
Sex: Female, Male
Male
12 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
EG002
affected / at risk
deaths
Total, all-cause mortality
0 / 220 / 220 / 22
other
Total, other adverse events
9 / 224 / 222 / 22
serious
Total, serious adverse events
0 / 220 / 220 / 22

Outcome results

Primary

Metformin AUC

Area under the plasma concentration time curve of metformin

Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.

Population: All 22 participants completed the 3 arms of the study (baseline, acute goldenseal exposure, and chronic goldenseal exposure).

ArmMeasureValue (GEOMETRIC_MEAN)
Study Arm 1: BaselineMetformin AUC59.6 mcg*hr/mL
Study Arm 2: Acute Goldenseal ExposureMetformin AUC54.5 mcg*hr/mL
Study Arm 3: Chronic Goldenseal ExposureMetformin AUC57.3 mcg*hr/mL
Comparison: The predefined no effect range was 0.80-1.25; that is, if the geometric mean ratio lay outside this range, a pharmacokinetic interaction was evident.90% CI: [0.82, 0.96]
Primary

Metformin Cmax

maximum concentration of metformin

Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.

ArmMeasureValue (GEOMETRIC_MEAN)
Study Arm 1: BaselineMetformin Cmax8.92 nM
Study Arm 2: Acute Goldenseal ExposureMetformin Cmax8.36 nM
Study Arm 3: Chronic Goldenseal ExposureMetformin Cmax8.26 nM
90% CI: [0.85, 1.01]
Secondary

Metformin Half-Life

half-life of metformin

Time frame: 0-24h

ArmMeasureValue (GEOMETRIC_MEAN)
Study Arm 1: BaselineMetformin Half-Life4.73 hours
Study Arm 2: Acute Goldenseal ExposureMetformin Half-Life4.70 hours
Study Arm 3: Chronic Goldenseal ExposureMetformin Half-Life4.79 hours
90% CI: [0.93, 1.07]
Secondary

Metformin Renal Clearance

renal clearance of metformin

Time frame: 0-24h

ArmMeasureValue (GEOMETRIC_MEAN)
Study Arm 1: BaselineMetformin Renal Clearance259 mL / min
Study Arm 2: Acute Goldenseal ExposureMetformin Renal Clearance249 mL / min
Study Arm 3: Chronic Goldenseal ExposureMetformin Renal Clearance250 mL / min
90% CI: [0.84, 1.12]
Secondary

Midazolam AUC

area under the concentration vs. time curve of midazolam

Time frame: Before and 20 minutes, 40 minutes, and 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 8, 10, and 12 hours after midazolam administration.

ArmMeasureValue (GEOMETRIC_MEAN)
Study Arm 1: BaselineMidazolam AUC31.9 mcg*hr/mL
Study Arm 2: Acute Goldenseal ExposureMidazolam AUC31.1 mcg*hr/mL
Study Arm 3: Chronic Goldenseal ExposureMidazolam AUC29.7 mcg*hr/mL
90% CI: [0.81, 1.15]

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026