University of Wisconsin
Madison, Wisconsin, 53706, United States
NCT Number: NCT07218653
This study tests the hypothesis that Metabolic Syndrome (MetSyn) decreases cerebral blood flow (CBF) more in females than males due in part to the sex-specific loss of COX vasodilation. Male and female participants will be enrolled in two groups: Healthy Controls versus participants with MetSyn.
Trial opening soon.
Get Notified18 year–45 year
All sexes
Interventional
Early Phase 1
Madison, Wisconsin, 53706, United States
The central hypothesis is that MetSyn decreases CBF more in females than males due in part to the sex-specific loss of COX vasodilation. This hypothesis is based on extensive preliminary data demonstrating MetSyn induces: 1) 3-fold larger reductions in CBF in females that abolish sex differences, 2) region-specific CBF reduction patterns, and 3) a greater loss of COX-mediated vasodilation in females.
This hypothesis is tested via three Specific Aims:
All consented participants will conduct a screening visit with a blood panel to identify control vs MetSyn eligibility.
Once eligible, participants complete three laboratory visits (each lasting about 2 hours):
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(Healthy Controls):
Inclusion criteria
(Participants with Metabolic Syndrome):
Exclusion criteria
(Healthy Controls):
Exclusion criteria
(all participants):
Indomethacin is a nonsteroidal anti-inflammatory. It prevents the production of prostaglandins, endogenous signaling molecules known to cause symptoms from inflammation.
Indomethacin (1.5 mg/kg) will be taken orally prior to one MRI study visit.
Other names: Indo
Participants will be screened for lactose intolerance. Total dosing will be calculated to match the mg needed for the indomethacin study visit.
Other names: Lactose
CBF testing will be performed on 3T MRI scanners (GE Healthcare)
Other names: Magnetic Resonance Imaging
Time frame: data collected over 2 study visits that must be completed within 6 months
Data collected via MRI under one of 2 conditions: placebo or indomethacin.
Time frame: data collected at one study visit (must be completed within 6 months)
Graded exercise test to assess maximal aerobic capacity, reported as VO2 max (milliliters of oxygen consumed per kilogram of body weight per minute)
Time frame: data collected at one study visit (must be completed within 6 months)
Dual-energy x-ray absorptiometry (DEXA) to measure fat mass.
Time frame: data collected at one study visit (must be completed within 6 months)
NIH Toolbox to assess neurocognitive function. The Flanker test is a measure of executive function and is scored using a T-score where 100 is the average, higher scores indicate better performance.
Time frame: data collected at one study visit (must be completed within 6 months)
NIH Toolbox to assess neurocognitive function. The Pattern Comparison Processing Speed Test measures how many correct responses the participant has within 90 seconds. There is a maximum of 130 items.
Time frame: data collected at one study visit (must be completed within 6 months)
NIH Toolbox to assess neurocognitive function. The List Sorting Working Memory Test is a measure of recall and sorting. Participants scores reflect the number of items recalled and appropriately sorted up to 28 items maximum.
Time frame: data collected at one study visit (must be completed within 6 months)
NIH Toolbox to assess neurocognitive function. The Dimensional Change Card Sort Test measures accuracy: the number of accurate responses, up to a maximum of 40.
Time frame: data collected at one study visit (must be completed within 6 months)
NIH Toolbox to assess neurocognitive function. The Picture Vocabulary Test has the participant hear a word and then pick from one of four pictures that best represents the word. It is scored using a T-score where 100 is the average, higher scores indicate better performance.
Contact information is provided by the study sponsor or research team.
University of Wisconsin, Madison
Other
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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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