caloric restriction - 10%
BehavioralSubjects maintained on 10% caloric restriction (caloric intake = 90% of baseline)
NCT Number: NCT00383253
Methods study to characterize early indicators of weight loss in people.
Looking for future studies?
Notify Me18 year–55 year
Male
Interventional
Not applicable
Pfizer Investigational Site, Adelaide, South Australia, Australia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Subjects maintained on 10% caloric restriction (caloric intake = 90% of baseline)
Subjects maintained on 25% caloric restriction (caloric intake = 75% of baseline)
Subjects maintained on 50% caloric restriction (caloric intake = 50% of baseline)
Subjects maintained on their baseline caloric intake (caloric restriction = none)
Time frame: Throughout trial
Time frame: Throughout trial
Looking for future studies?
Notify MePfizer
Industry
A Randomized, Open-Label, Parallel Group, Fixed Energy Deficit Methodology Trial to Characterize Early Efficacy Biomarkers During Treatment of Obesity in Adult, Obese, Male Subjects.
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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.
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