Could date seed powder help tame type 2 diabetes?
NCT ID NCT07702097
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This study tests whether a daily 4-gram dose of ajwa seed powder, made from date seeds, can improve blood sugar control (HbA1c) and body composition in overweight and obese adults aged 30–50 with type 2 diabetes. Over 12 weeks, researchers will measure changes in HbA1c, weight, waist and hip circumference, and fat levels. The goal is to see if this natural supplement offers a simple way to help manage diabetes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ajwa seed powder, a natural dietary supplement from date seeds
- What this could lead to
- If effective, ajwa seed powder could offer a simple, natural supplement to help manage blood sugar and body weight in type 2 diabetes.
- What could go wrong
- This is a small, early trial with no control group, so results may not be conclusive. The supplement is unregulated and long-term safety is unknown.
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
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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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
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30 to 50 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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 * Age: 30-50 years * Gender: Male/female * Body Mass Index (BMI): 25-35 kg/m² * Type 2 diabetes mellitus: HbA1c ≥ 6.5% Exclusion criteria History of alcoholic liver disease or cirrhosis; liver dysfunction based on initial blood tests * Patients being treated with insulin * High initial levels of serum creatinine (men\>1.5 mg/dl; women\>1.2 mg/dl) * Pregnant/lactating females or women who cannot take proper contraceptive measures * Symptoms consistent with peptic ulcer disease or history of peptic ulcers * Active cancer patients * Severe non-diabetes-related illnesses * Patients with heart, liver, or lung failures * Patients with blood disorders or on anticoagulant drugs such as warfarin Any other disease as decided by the principal investigator, which might put the safety of the subjects at risk while conducting the test
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Sultan Hospital
Sheikhupura, 39359, Pakistan
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Other studies related to the condition(s) this trial covers.
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