Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05025865

HA35 Acute Alcohol Study

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.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Cleveland Clinic

Cleveland, Ohio, 44195, United States

Location status: Recruiting

Location contact

Annette Bellar

CONTACT

[email protected]

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

  • 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

Treatment and study plan

Sodium Hyaluronate

Drug

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

Other names: HA35

Placebo

Drug

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

Primary outcomes

  1. Change in Aspartate Aminotransferase (AST)

    Time frame: Baseline to day 4

    change in units/liter (U/L)

  2. Change in Alanine Aminotransferase (ALT)

    Time frame: Baseline to day 4

    change in units/liter (U/L)

Study contacts

Contact information is provided by the study sponsor or research team.

Annette Bellar

CONTACT

[email protected]

Srinivasan Dasarathy, MD

CONTACT

[email protected]

216-318-7010

Sponsors and collaborators

Lead sponsor

The Cleveland Clinic

Other

Registry information

Official study title

Mechanisms by Which HA35 Regulates Muscle Protein Homeostasis in Healthy Controls

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Aug 27, 2021
Registry last updated
Nov 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.