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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03225677
Other study ID # 14-1476
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 3, 2017
Est. completion date September 30, 2024

Study information

Verified date September 2023
Source The Cleveland Clinic
Contact Annette Bellar, MSLA
Phone 2164450688
Email bellara@ccf.org
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To determine the rate and mechanisms of skeletal muscle protein synthesis and breakdown in cirrhotic patients by using multiple tracers and single muscle biopsies.


Description:

The goal of this study is to identify the molecular regulatory mechanisms that result in loss of skeletal muscle in cirrhotic patients. Current strategies involve prolonged tracer infusion and multiple muscle biopsies. We will use an innovative approach to determine the rates of skeletal muscle protein synthesis and breakdown using multiple tracers administered at short intervals followed by a single muscle biopsy. These studies are likely to provide a conceptual advance in determining the cellular and molecular responses of the skeletal muscle in cirrhosis.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date September 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The diagnosis of cirrhosis based on liver biopsy and/or clinical, biochemical, and imaging criteria. - Patients with Child Pugh score from A5- to B7 - Control group: Subject in control group should have serum ALT and AST within normal range. Exclusion Criteria for both groups (cirrhotic and control) are: - diabetes - cancer - kidney failure - pregnancy - recent surgery (bowel resection or Gastric bypass operation) - Advanced cardiac or pulmonary disease - patient with thyroid disease & Coagulopathy ( INR >1.4 and platelet count <80,000/ml)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
blood draw and muscle biopsy
One venous catheter will be used for bolus injection of multiple labeled AA at the beginning .The second venous catheter will inserted in the other arm for 5 ml of arterialized venous blood draw.Following the infusions, a single muscle biopsy will be performed from the vastus lateralis of the thigh using the Bergstromm needle.

Locations

Country Name City State
United States Cleveland Clinic Foundation Cleveland Ohio

Sponsors (1)

Lead Sponsor Collaborator
The Cleveland Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fractional Synthesis Rate Fractional synthesis rate (FSR)for each patient is measured by the rate of tracer incorporation from the MIF pool to the bound pool. 4 hours
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