CClinicalTrials.gg
RecruitingNCT05025865Updated Sep 24, 2026

HA35 Acute Alcohol Study

An Early Phase 1 interventional study of Sodium Hyaluronate and Placebo in Healthy Controls, sponsored by The Cleveland Clinic. Recruiting at 1 site in United States. Open to participants aged 21 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-24.

Sponsored by The Cleveland Clinic · Early Phase 1, Interventional, and Basic science

Phase
Early Phase 1
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
21 Years to 65 Years
Sex
All
01

Study summary

Eligible subjects will be asked to take a placebo/treatment capsule for a total of 3 days and then participate in a study visit on the fourth day. This study visit will include a medical exam, clinical labs, questionnaires, body composition measurements, and urine and stool collections. Additionally, participants will consume a sugar cocktail to measure their gut permeability, participate in an acute ethanol challenge, and undergo two muscle biopsies. The study will take approximately 3-4 hours and a designated driver will need to drive the participant home. On the fifth day, you will be asked to return to drop of the 24-hour urine collection.

Read the detailed description

Interested subjects will be assessed for eligibility and a written informed consent will be obtained. The screening visit will consist of a medical exam, clinical labs (if not available in medical record), and questionnaires. Those who pass the screening will be eligible for a baseline visit (may be combined with screening if appropriate labs are already done). The baseline visit will include collection of blood, urine, and stool samples, body composition measurements, and randomization into either HA35 or placebo groups. Patients will be instructed to take the HA35 or placebo daily in the morning before breakfast 3 days prior to the day 4 visit. Patients will be informed that they will need to have a driver that is known to them for the day 4 visit. In the morning of the day 4 visit, confirmation of a driver will occur prior to starting study procedures. During the day 4 visit, patients will have an acute ethanol challenge where they will need to consume 2mL/kg of vodka in 100mL of juice in under 60 minutes. Muscle biopsies will be collected before and after the challenge and blood will be collected throughout the day. In addition, patients will be given lactulose/mannitol/sucralose/sucrose cocktail to measure gut permeability. The costs of any of these tests/procedures will not be billed to the patient and will be covered by the department. The participant will not be responsible for any costs.

02

Conditions studied

  • Healthy Controls
03

Who can participate

Ages eligible
21 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Alcohol consumption of less than 7 drinks per week for women and less than 14 drinks per week for men
  • Ability to understand and willingness to provide written consent

Exclusion criteria

Exclusion Criteria:

  • Any known chronic illness including but not limited to cancer (except non-melanoma skin cancer)
  • Poorly controlled diabetes (Hemoglobin A1c >9.5 g/dl)
  • Untreated hyper/hypothyroidism
  • Uncontrolled hypertension or hypercholesterolemia
  • End-stage renal disease
  • Liver disease of any etiology
  • Coronary artery disease or stroke
  • Active intravenous drug use
  • History of gastric bypass
  • Medications known to alter muscle protein synthesis (systemic corticosteroids, tamoxifen, high dose estrogen, testosterone, or anabolic steroids)
  • Pregnancy
  • Past alcohol use disorder
  • Abnormal clotting factors
04

Study design

Phase
Early Phase 1
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
24 participants (estimated)

Study arms

  • Placebo comparator
    HA35 Placebo Group

    12 study participants will be given a placebo capsule to take once per day in the morning with breakfast for 3 days.

    Drug: Placebo

  • Active comparator
    HA35 Treatment Group

    12 study participants will be given an HA35 capsule to take once per day in the morning with breakfast for 3 days.

    Drug: Sodium Hyaluronate

Interventions

  • DrugSodium Hyaluronate

    Sodium Hyaluronate of molecular weight 35 kDa will be given in capsule form to the study participants.

    Also known as: HA35

  • DrugPlacebo

    A placebo will be given in capsule form to study participants.

05

What researchers measure

Primary outcomes

  1. Change in Aspartate Aminotransferase (AST)

    change in units/liter (U/L)

    Time frame: Baseline to day 4

  2. Change in Alanine Aminotransferase (ALT)

    change in units/liter (U/L)

    Time frame: Baseline to day 4

06

Study locations

1 of 1 sites recruiting
  • Cleveland Clinic
    Cleveland, Ohio 44195, United States
    Recruiting
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT05025865
Lead sponsor
The Cleveland Clinic
Responsible party
Srinivasan Dasarathy (Staff Physician, The Cleveland Clinic) — Principal investigator
First posted
Aug 27, 2021
Start date
Feb 1, 2022
Primary completion
Oct 1, 2028 (estimated)
Completion
Oct 1, 2028 (estimated)
Last update
Sep 24, 2026

Study contacts

Srinivasan Dasarathy, MD
Contact
dasaras@ccf.org
216-318-7010
Annette Bellar
Contact
bellara@ccf.org

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion