AzTrials
AzTrials

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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

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.

United States1 site
  • Medinutra LLC

    Dublin, Ohio, 43016

Other trials in United States

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 groups in NCT07101263
Study groupRoleWhat they receive
Standard wheyPlacebo comparatorA standard whey protein is consumed daily for 6 weeks
Receives: Dietary Supplement: Standard whey
Hydrolyzed wheyExperimentalA 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.

  1. Serum cholesterol

    Serum total and LDL cholesterol (mg/dL) will be assessed

    Measured: 6 weeks

Secondary outcomes (2)
  1. 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

  2. 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.

  1. First posted3 Aug 2025
  2. Study start5 Aug 2025
  3. Primary completion10 Jul 2026
  4. Study completion10 Jul 2026

Resources

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)
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

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.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in