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Alterations in Protein Synthesis Rates of Burn Patients Measured Over Time Using PET Scans

A Quantitative Study of the Metabolic Alterations in Protein Synthesis Rate That Occur in Burn Patients Over the Time Course of Their Injury Using Positron Emission Tomography.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00253279
Enrollment
64
Registered
2005-11-15
Start date
2009-11-30
Completion date
2010-01-31
Last updated
2009-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burn

Keywords

Protein Synthesis Rate, Burn Injury, PET Scan

Brief summary

Our specific aim is to gain an understanding of protein synthesis rates in burn patients at various times during their injury and recovery by using PET scans. This will be compared with healthy volunteer controls. We hope this will help optimize nutrition and care regimens for future burn patients.

Detailed description

The purpose of this study is to understand how muscles are built up and broken down (metabolism) in both burn patients and healthy people.The studies will help us understand how muscle metabolism is different for burn patients and healthy subjects. We hope to find ways to help the body of a burn victim heal without losing too much muscle. Protein is an important part of our daily diet. Normally, the body breaks down the protein we eat into smaller pieces called amino acids. It uses the amino acids to make its own proteins. It uses these proteins to heal wounds, fight infections, and provide energy. After a burn injury, the body speeds up the pace of its life activities. It needs more energy just to stay alive and recover from the burn. The body often gets the extra energy it needs by breaking the protein in muscles down into amino acids. The amino acids are then made into new proteins. If too much muscle is broken down, it is harder for the body to function. This can make recovery slower or possibly lead to death. For Healthy Volunteers, this study will require no more than 6 hours of time in total. This time will be spread out over two visits, a Screening Visit and a Scan Visit. For Burn Patients, this study will require no more than 14 hours total. This time will be spread out over four visits-a screening visit and a maximum of 3 scan visits. A total of three PET scans will be done over a 2 year period.

Interventions

PROCEDUREPET Scans

Healthy volunteers will undergo one PET Scan; bur patients will undergo a maximum of 3 PET scans over 2 years after injury; a maximum of 2 will be done while inpatient; one after d/c.

Sponsors

National Institute of General Medical Sciences (NIGMS)
CollaboratorNIH
Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

FOR HEALTHY VOLUNTEERS Healthy males and females 18-70 years of age. Laboratory results within MGH-accepted normal range. Within 20% of the ideal weight for their height. Supine and standing blood pressure within the range of 110/60 to 150/90 mm Hg Heart rate within the range of 46-90 beats/minute after 5 minutes of rest. Subjects \<40 years old with HCT \>=24, age 40-60 with HCT \>=27, age 60-70 with HCT \>=30. FOR BURN SUBJECTS: Inclusion Criteria: Burn Injury of \>=5 % TBSA from any cause. 18 -70 years of age Stable hemodynamic and cardiopulmonary states as judged by the attending surgeons in the burn unit. Patient who is capable of giving full informed consent.

Exclusion criteria

FOR HEALTHY SUBJECTS Clinical evidence of physical or mental disease. Clinically significant abnormality of the laboratory tests. Known drug or alcohol dependence. History of drug allergy Taking standard prescription drugs within two weeks or investigational drugs within four weeks prior to the PET scan Diabetes mellitus and other metabolic endocrine disorders Pregnant or lactating FOR BURN SUBJECTS: Pregnant or lactating females

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026