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Cofactor
Tetrahydrobiopterin for Chronic Obstructive Pulmonary Disease
Phase 1
Waitlist Available
Research Sponsored by University of Massachusetts, Amherst
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 hours
Awards & highlights
Study Summary
This trial looks at how well a treatment works in people with COPD who also have skeletal muscle dysfunction.
Eligible Conditions
- Chronic Obstructive Pulmonary Disease
- Tetrahydrobiopterin Deficiency
- Stress Oxidative
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 hours
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 hours
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mitochondrial function
intracellular PO2
Secondary outcome measures
Peripheral Blood flow
systemic blood markers of oxidative stress
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: acute BH4/Tetrahydrobiopterin treatmentExperimental Treatment1 Intervention
Oral supplement, Pill, 10 mg/kg of body weight
Group II: PlaceboPlacebo Group1 Intervention
Oral supplement, Pill, Placebo pill with inert excipient
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Sapropterin
FDA approved
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
University of Massachusetts, AmherstLead Sponsor
78 Previous Clinical Trials
467,772 Total Patients Enrolled
Frequently Asked Questions
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