CholesterolNCT07101263
Whey Protein Comparisons for Blood Lipid Effects
A study testing Standard whey and Hydrolyzed whey in people with Cholesterol, run by Medinutra LLC at 1 site in United States.
Trial summary
The goal of this clinical trial is to learn if hydrolyzed whey protein can help serum cholesterol stay in normal range in adults. As a side inquiry, a few blood measures will be taken that are relevant to low level inflammation. Read more about this study
- Who is it for?
- Ages 21 to 59 yearsHealthy volunteers can take part
- Conditions the study is for
- Cholesterol
- What is being tested?
- Standard whey and Hydrolyzed whey
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 60 participants
- Where
- 1 siteUnited States
- Study dates
- 5 Aug 2025to 10 Jul 2026
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 to 59 years
- All sexes
- Healthy volunteers accepted
- Adult
Who may be able to join
- Cholesterol reading of 190 to 225 mg/dL
- Age 21-59 years old
Who cannot join
- Uncontrolled diabetes
- Hypothyroidism or other hormonal problems that have not stabilized
- Any liver diseases being actively treated
- Cancer
- Renal dialysis use
- Rheumatoid arthritis and related issues like lupus
Show all 16Show fewer
- Inflammatory bowel disease
- Smoking
- Following a very restrictive diet
- Low blood pressure
- Statin drug use
- Having more than 5 alcoholic drinks per week
- Extreme obesity (BMI over 37)
- Pregnancy or lactation
- Allergies to milk protein
- History of discomfort after consuming whey protein
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Hydrolyzed Whey for Blood Lipid Control
The goal of this clinical trial is to learn if hydrolyzed whey protein can help serum cholesterol stay in normal range in adults. As a side inquiry, a few blood measures will be taken that are relevant to low level inflammation. The main questions the study aims to answer are:
- Will hydrolyzed whey lower serum cholesterol readings in adults with starting values in the upper end of normal to the lower end of elevated?
- Will the hydrolyzed whey affect a general measure of inflammation and two measures of indirect relevance to inflammation?
Read more
Researchers will compare hydrolyzed whey to a conventional whey (a control protein not expected to affect serum cholesterol readings) to see if the hydrolyzed whey lowers serum cholesterol.
Participants will:
- Drink one protein beverage every day for 6 weeks;
- Go to a LabCorp facility for a blood draw before and after the 6 weeks.
Read the detailed description
Background. According to the American Medical Association and the Centers for Disease Control, nearly 94 million adults over the age of 20 have what could be considered borderline high cholesterol. Most of these people don't take drugs to lower cholesterol. Therefore, this group of people represent a target for other approaches to lowering cholesterol readings. This group can include people in the high end of acceptable range since they can run the risk of getting into borderline high readings. A nutritional product could be part of a plan to keep cholesterol readings in the normal range.
Whey protein could comprise such a product. This protein gets used in many protein powders, ready-to-drink beverages and bars. However, whey does not have a simple and consistent record for lowering cholesterol readings. Even with the studies giving positive results, only indirect effects may occur. This can happen by whey replacing fat and high glycemic index carbohydrate foods, or by impacting satiety.
In contrast, this project tests the proposition that certain versions of hydrolyzed whey can directly exert a modest but useful action on cholesterol readings. The applicant has found this in a small unpublished study in older exercisers. In addition, a retracted study has shown that in people with pre-hypertension or moderate hypertension, hydrolyzed whey can reduce total and LDL cholesterol readings. A decrease of 29 mg/dL for total cholesterol despite only moderately high starting cholesterol values).
Although this data is useful, it is based only an unpublished study and a retracted paper. Also, the two populations studied were somewhat narrow. Thus, a new study is now going to be done in a fairly broad population. Positive results in this and possible subsequent research could be applied to products quickly since no drug claim is needed. The Dietary Supplement and Education Act (DSHEA) allows for structure function claims of helping maintain blood lipids in the normal range.
As a side note, hydrolyzed whey protein could also reduce low level general inflammation. This process, which falls below what's seen with inflammatory diseases or injury, can raise the risk for many long term health problems. Drugs are not generally employed to minimize this type of inflammation. So, as with moderately high TG readings, relatively safe and inexpensive non-drug alternatives can be sought (including nutritional supplements).
Methods. Subjects will be adult males and females aged 21-59 that lack unstable health problems that can affect cholesterol or systemic inflammation readings. Subjects in this project will have starting total cholesterol reading of 190-225 mg/dL. Initially, this eligibility will be based on eligibility questionnaire. However, if the initial blood draw finds cholesterol readings outside the range, subjects will be excluded and replaced. Other discontinuations will be for a subject's decision or a change in health or medication disclosed by the subject to Medinutra. For these discontinuations, subjects will not be replaced (see next section).
For 6 weeks, subjects will take one of the following orally as one serving/day (up to16 people/group):
Hydrolyzed whey (Hilmar) 25g protein/day Whey protein isolate (Hilmar) 25g protein/day
Blood will be drawn and analyzed at a LabCorp facility. The blood draw site will vary according to the location where each subject lives. Neither Labcorp nor the study subjects will not know the assigned protein identity. Thus, this will be double blinded and randomized in terms of the participants and analyzers
Measures will consist of blood lipids and three measures directly or indirectly related to low level inflammation. For each measure, for each of the 2 treatment groups, pre- and post-treatment values will be compared by paired t-test. In addition, the changes in values for each group will be compared to each group by unpaired t-test. For non-normal distribution, nonparametric tests can be used. Significance for all analysis is set at p < 0.05.
Subject numbers and power calculation. Subject number will be 36/group. For a power calculation, for hydrolyzed whey alone, the 7% change in total cholesterol from the applicant pilot study is used as the minimal desired change. The comparison protein is assumed to have about a 0% change. The variation is set at 4.8%. This produces a power value of 0.95 with a two way p value of 0.01 for 34 subjects per group. An extra 2 subjects per group will be added in case of dropouts. Dropouts are not expected to happen at a high rate since only two trips are required to a site, drinking a protein beverage is not overly hard, and subjects will not be able to tell if an effect is occurring during the study. In the last regard, this study does not resemble something like osteoarthritis research where non-improving pain can make a person drop out.
Safety considerations. Ingestion of any type of beverage as well as having blood draws have some risks, but major risks are not common. The main concern of this study is allergies to whey protein. If someone has allergies to whey, then allergies to milk proteins would also be expected. Therefore, if someone has had milk allergies, then they should not participate in the study. Some people have claimed that allergies to whey can show up even if milk protein allergies exist, but this contention lacks confirmation. However, if a person has ever had any discomfort after consuming whey, then they should not participate.
- Conditions
- Cholesterol
- Being tested
- Standard whey, Hydrolyzed whey
- Keywords
- Cholesterol, Whey, inflammation, Moderately elevated cholesterol, High end normal cholesterol
- Medical subject headings
- Inflammation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Standard wheyDietary supplement
A typical whey protein is given that differs in chemical structure from the atypical whey protein used in the experimental group
Hydrolyzed wheyDietary supplement
This type of whey has different chemical structure from typical wheys such as that used in this nstudy's control group
| Study group | Role | What they receive |
|---|---|---|
| Standard whey | Placebo comparator | A standard whey protein is consumed daily for 6 weeks Receives: Dietary Supplement: Standard whey |
| Hydrolyzed whey | Experimental | A hydrolyzed whey protein is consumed daily for 6 weeks Receives: Dietary Supplement: Hydrolyzed whey |
What is being measured
The primary outcome is the main question the study is designed to answer.
Serum cholesterol
Serum total and LDL cholesterol (mg/dL) will be assessed
Measured: 6 weeks
Secondary outcomes (2)
Other Blood Lipids
Serum HDL cholesterol and triglycerides (mg/dL) will be assessed, but mean values are not expected to change in either group
Measured: 6 weeks
Inflammation markers
As a secondary consideration, this study will assess 3 blood measures relevant to low level inflammation: serum c reactive protein (mg/dL), serum alanine aminotransferase (ALT-Units/L), and whole blood glutathione (mg/L)
Measured: 6 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Aug 2025
- Study start5 Aug 2025
- Primary completion10 Jul 2026
- Study completion10 Jul 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for CholesterolStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Medinutra LLC
- Sponsor type
- University, hospital or other
- Collaborators
- Dairy Management Inc.
- Responsible party
- Principal investigator, Robert DiSilvestro, Medinutra LLC
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07101263
- Sponsor's protocol ID
- Medinutra002
- Status last verified
- Aug 2025
- First submitted
- 28 Jul 2025
- Last updated
- 14 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Pins JJ, Keenan JM. Effects of whey peptides on cardiovascular disease risk factors. J Clin Hypertens (Greenwich). 2006 Nov;8(11):775-82.
PubMed 17086017
Study at a glance
From the registry record, last updated by the sponsor on 14 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Hydrolyzed Whey for Blood Lipid Control
- ClinicalTrials.gov ID
- NCT07101263
- Acronym / sponsor ID
- Medinutra002
- Conditions
- Cholesterol
- Keywords
- Cholesterol, Whey, inflammation, Moderately elevated cholesterol, High end normal cholesterol
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Medinutra LLCUniversity, hospital or other
- Collaborators
- Dairy Management Inc.
- Study start
- 5 Aug 2025 (actual)
- Primary completion
- 10 Jul 2026 (actual)
- Study completion
- 10 Jul 2026 (actual)
- First posted
- 3 Aug 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this clinical trial is to learn if hydrolyzed whey protein can help serum cholesterol stay in normal range in adults. As a side inquiry, a few blood measures will be taken that are relevant to low level inflammation. The main questions the study aims to answer are:
- Will hydrolyzed whey lower serum cholesterol readings in adults with starting values in the upper end of normal to the lower end of elevated?
- Will the hydrolyzed whey affect a general measure of inflammation and two measures of indirect relevance to inflammation?
Researchers will compare hydrolyzed whey to a conventional whey (a control protein not expected to affect serum cholesterol readings) to see if the hydrolyzed whey lowers serum cholesterol.
Participants will:
- Drink one protein beverage every day for 6 weeks;
- Go to a LabCorp facility for a blood draw before and after the 6 weeks.
Detailed description
Background. According to the American Medical Association and the Centers for Disease Control, nearly 94 million adults over the age of 20 have what could be considered borderline high cholesterol. Most of these people don't take drugs to lower cholesterol. Therefore, this group of people represent a target for other approaches to lowering cholesterol readings. This group can include people in the high end of acceptable range since they can run the risk of getting into borderline high readings. A nutritional product could be part of a plan to keep cholesterol readings in the normal range.
Whey protein could comprise such a product. This protein gets used in many protein powders, ready-to-drink beverages and bars. However, whey does not have a simple and consistent record for lowering cholesterol readings. Even with the studies giving positive results, only indirect effects may occur. This can happen by whey replacing fat and high glycemic index carbohydrate foods, or by impacting satiety.
In contrast, this project tests the proposition that certain versions of hydrolyzed whey can directly exert a modest but useful action on cholesterol readings. The applicant has found this in a small unpublished study in older exercisers. In addition, a retracted study has shown that in people with pre-hypertension or moderate hypertension, hydrolyzed whey can reduce total and LDL cholesterol readings. A decrease of 29 mg/dL for total cholesterol despite only moderately high starting cholesterol values).
Although this data is useful, it is based only an unpublished study and a retracted paper. Also, the two populations studied were somewhat narrow. Thus, a new study is now going to be done in a fairly broad population. Positive results in this and possible subsequent research could be applied to products quickly since no drug claim is needed. The Dietary Supplement and Education Act (DSHEA) allows for structure function claims of helping maintain blood lipids in the normal range.
As a side note, hydrolyzed whey protein could also reduce low level general inflammation. This process, which falls below what's seen with inflammatory diseases or injury, can raise the risk for many long term health problems. Drugs are not generally employed to minimize this type of inflammation. So, as with moderately high TG readings, relatively safe and inexpensive non-drug alternatives can be sought (including nutritional supplements).
Methods. Subjects will be adult males and females aged 21-59 that lack unstable health problems that can affect cholesterol or systemic inflammation readings. Subjects in this project will have starting total cholesterol reading of 190-225 mg/dL. Initially, this eligibility will be based on eligibility questionnaire. However, if the initial blood draw finds cholesterol readings outside the range, subjects will be excluded and replaced. Other discontinuations will be for a subject's decision or a change in health or medication disclosed by the subject to Medinutra. For these discontinuations, subjects will not be replaced (see next section).
For 6 weeks, subjects will take one of the following orally as one serving/day (up to16 people/group):
Hydrolyzed whey (Hilmar) 25g protein/day Whey protein isolate (Hilmar) 25g protein/day
Blood will be drawn and analyzed at a LabCorp facility. The blood draw site will vary according to the location where each subject lives. Neither Labcorp nor the study subjects will not know the assigned protein identity. Thus, this will be double blinded and randomized in terms of the participants and analyzers
Measures will consist of blood lipids and three measures directly or indirectly related to low level inflammation. For each measure, for each of the 2 treatment groups, pre- and post-treatment values will be compared by paired t-test. In addition, the changes in values for each group will be compared to each group by unpaired t-test. For non-normal distribution, nonparametric tests can be used. Significance for all analysis is set at p < 0.05.
Subject numbers and power calculation. Subject number will be 36/group. For a power calculation, for hydrolyzed whey alone, the 7% change in total cholesterol from the applicant pilot study is used as the minimal desired change. The comparison protein is assumed to have about a 0% change. The variation is set at 4.8%. This produces a power value of 0.95 with a two way p value of 0.01 for 34 subjects per group. An extra 2 subjects per group will be added in case of dropouts. Dropouts are not expected to happen at a high rate since only two trips are required to a site, drinking a protein beverage is not overly hard, and subjects will not be able to tell if an effect is occurring during the study. In the last regard, this study does not resemble something like osteoarthritis research where non-improving pain can make a person drop out.
Safety considerations. Ingestion of any type of beverage as well as having blood draws have some risks, but major risks are not common. The main concern of this study is allergies to whey protein. If someone has allergies to whey, then allergies to milk proteins would also be expected. Therefore, if someone has had milk allergies, then they should not participate in the study. Some people have claimed that allergies to whey can show up even if milk protein allergies exist, but this contention lacks confirmation. However, if a person has ever had any discomfort after consuming whey, then they should not participate.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Standard whey | Placebo comparator | Dietary Supplement: Standard wheyA standard whey protein is consumed daily for 6 weeks |
| Hydrolyzed whey | Experimental | Dietary Supplement: Hydrolyzed wheyA hydrolyzed whey protein is consumed daily for 6 weeks |
Who may qualify
- Ages
- 21 to 59 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- Cholesterol reading of 190 to 225 mg/dL
- Age 21-59 years old
Key exclusion criteria (16 listed)
- Uncontrolled diabetes
- Hypothyroidism or other hormonal problems that have not stabilized
- Any liver diseases being actively treated
- Cancer
- Renal dialysis use
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Standard wheyA typical whey protein is given that differs in chemical structure from the atypical whey protein used in the experimental group | Dietary supplement | Standard whey |
| Hydrolyzed wheyThis type of whey has different chemical structure from typical wheys such as that used in this nstudy's control group | Dietary supplement | Hydrolyzed whey |
Primary outcome
Serum cholesterol
Time frame: 6 weeks
Serum total and LDL cholesterol (mg/dL) will be assessed
2 secondary outcomes
Other Blood Lipids
Time frame: 6 weeks
Inflammation markers
Time frame: 6 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jul 2026.
- Results publication: PubMed 17086017Pins JJ, Keenan JM. Effects of whey peptides on cardiovascular disease risk factors. J Clin Hypertens (Greenwich). 2006 Nov;8(11):775-82.
- The American Medical Association and the Centers for Disease Control reported that nearly 94 million adults over the age of 20 have what could be considered borderline high cholesterolLink provided by the sponsor.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Standard whey and Hydrolyzed whey in people with Cholesterol, run by Medinutra LLC at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Serum cholesterol (time frame: 6 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07101263, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jul 2026.