Ashwagandha safety check in seniors: small study ends early
NCT ID NCT06171724
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study aimed to measure how a standardized ashwagandha supplement is absorbed and tolerated in healthy adults aged 65 and older. Eleven participants took either 240 or 480 mg of the supplement, and researchers tracked levels of active compounds in the blood over 48 hours. The study was terminated early, so the findings are limited to basic safety and absorption data.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ashwagandha (Withania somnifera) extract
- What this could lead to
- If successful, this could provide basic information on how ashwagandha is absorbed and tolerated in older adults, potentially guiding future studies on its health effects.
- What could go wrong
- This was a very small, early-phase study that was terminated, so results are limited. It only looked at safety and absorption, not whether ashwagandha has any health benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
-
11 people
The number who actually took part.
- Started
-
Apr 2024
- Finished
-
Dec 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
65 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 65 and older, male and female 2. Body Mass Index (BMI) greater than 17 and less than 35 at screening 3. Sufficient vision and hearing to complete all tests 4. Willingness to discontinue all botanical supplementation for one week prior to and throughout study 5. No known sensitivity to Withania somnifera or any of its derivatives 6. Normal or clinically not significant 12-lead electrocardiogram (ECG) recording 7. Hepatic (ALT, AST, bilirubin), renal (creatinine, estimated GFR), and TSH parameters within normal range 8. Hemoglobin ≥13.0 g/dL or hematocrit ≥39% (males) OR hemoglobin ≥12.5 g/dL or hematocrit ≥38% (females), per FDA recommendations on blood donation 9. General health status that will not interfere with the ability to complete the study 10. Willingness to attend all study visits 11. Willingness to avoid caffeine and xanthine-containing foods or beverages (e.g., coffee, tea, chocolate, caffeine-containing sodas, colas, etc.), as well as grapefruit juice and poppy-containing foods for 48 hours prior to baseline visits 12. Willingness to adhere to special diet (no dairy, grapefruit products, poppy-containing foods, high-fat meals, caffeine, or xanthine-containing foods or beverages) during baseline visits and until after 24-hour visit 13. Mini-Mental State Exam (MMSE) score ≥26 Exclusion Criteria: 1. Current smoking, alcohol, or substance abuse according to DSM-V criteria 2. Participants who are currently pregnant, actively trying to conceive a child, or planning to within three months of study completion 3. Severe aversion to venipuncture 4. Donation of blood within 90 days of screening 5. Participation in drug research study within 90 days of screening 6. Serious health condition (i.e., illness, injury, impairment, or physical or mental condition which requires a) overnight hospitalization or b) continuing treatment that may cause episodic periods of incapacity of more than 3 consecutive days) within 30 days of screening 7. Allergy to nightshade plants (Solanaceae family) 8. Abnormal labs indicating symptomatic and untreated urinary tract infection 9. History of prostate cancer 10. History of kidney transplant 11. Cancer within the last five years, with the exception of non-metastatic skin cancers 12. Comorbid conditions requiring medication such as diabetes, kidney failure, liver failure, hepatitis, blood disorders, hypotension, thyroid disease, respiratory disorders, or cardiovascular disease 13. Presence of sleep apnea, moderate to severe restless leg syndrome, major circadian rhythm changes, or narcolepsy 14. Significant disease of the Central Nervous System (CNS) such as brain tumor, seizure disorder, subdural hematoma, cranial arteritis, or clinically significant stroke 15. Diagnosis of major depression, schizophrenia, bipolar disorder, or other major psychiatric disorder as defined by DSM-V criteria 16. Diseases associated with dementia such as Alzheimer's disease, vascular dementia, normal pressure hydrocephalus or Parkinson's disease
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Oregon Health & Science University
Portland, Oregon, 97239, United States
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