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Last Updated: April 20, 2024

CLINICAL TRIALS PROFILE FOR ALBUMIN IODINATED I-131 SERUM


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All Clinical Trials for albumin iodinated i-131 serum

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00922194 ↗ Metformin in Overweight Type 2 Diabetes Mellitus Completed Era's Lucknow Medical College N/A 2006-02-01 The study included 102 overweight type 2 diabetes mellitus patients with a body mass index (BMI) of more than 25 in an open label study. They were advised intensive life style modification which was reinforced at each follow-up visit. In addition they were prescribed extended release metformin (XR) in a gradually increasing tolerable dose, starting with 0.5g twice a day after meals. In addition, hypertension and dyslipidemia, when present, were treated with appropriate recommended drugs. Those who completed a satisfactory regular follow-up for at least 12 months or more were then analyzed for changes in their anthropometric measurements and glycemic control.
NCT01544036 ↗ Monitoring Renal Blood Flow With Contrast Enhanced Ultrasound During Coronary Angiogram Unknown status National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) N/A 2012-02-01 Contrast induced nephropathy (CN) is a common cause of acute kidney injury and is associated with increased morbidity and mortality and healthcare cost. Iodinated contrast media (ICM) induce kidney injury through vasoconstriction and ischemia as well as direct tubular toxicity. Older subjects, individuals with preexisting kidney disease, diabetes, hypotension, and those exposed to higher volumes of ICM are at higher risks for CN. Within the last several years, multiple strategies have been used in clinical studies to reduce the risk of CN in high risk individuals with inconsistent results. In general, it is agreed that volume expansion is effective in reducing the risk. However, no study has looked at changes in renal blood flow (RBF) in response to volume expansion or after exposure to ICM to investigate its relationship with occurrence of CN. In this proposal, up to 125 individuals with preexisting kidney disease as evidenced by an estimated glomerular filtration rate (eGFR) between 30 - 60 ml/min/1.73 m2 and up to 25 individuals with normal renal function (total of up to 150 individuals) who are scheduled for coronary angiography will be studied. Each individual will have serial measurements of RBF; at baseline, after volume expansion with normal saline, and after exposure to ICM, using the novel technique of contrast enhanced ultrasound (CEU). The investigators will investigate the utility of monitoring RBF with CEU in predicting the occurrence of CN (a rise of > 0.3 mg/dL or 25% in baseline serum creatinine 48 hours after exposure to ICM) after adjusting for other known risk factors in the group of subjects with reduced GFR. The investigators will also examine the correlation between RBF changes and other urinary and serum biomarkers of kidney injury in this group. Up to 25 individuals with a normal kidney function will be studied in a separate part of the study in which the accuracy of CEU based measurements of RBF will be compared to the RBF and blood flow velocity obtained simultaneously using a Doppler flow probe placed directly inside the main renal artery during coronary angiogram procedure. Total to enroll = 150.
NCT01544036 ↗ Monitoring Renal Blood Flow With Contrast Enhanced Ultrasound During Coronary Angiogram Unknown status University of Virginia N/A 2012-02-01 Contrast induced nephropathy (CN) is a common cause of acute kidney injury and is associated with increased morbidity and mortality and healthcare cost. Iodinated contrast media (ICM) induce kidney injury through vasoconstriction and ischemia as well as direct tubular toxicity. Older subjects, individuals with preexisting kidney disease, diabetes, hypotension, and those exposed to higher volumes of ICM are at higher risks for CN. Within the last several years, multiple strategies have been used in clinical studies to reduce the risk of CN in high risk individuals with inconsistent results. In general, it is agreed that volume expansion is effective in reducing the risk. However, no study has looked at changes in renal blood flow (RBF) in response to volume expansion or after exposure to ICM to investigate its relationship with occurrence of CN. In this proposal, up to 125 individuals with preexisting kidney disease as evidenced by an estimated glomerular filtration rate (eGFR) between 30 - 60 ml/min/1.73 m2 and up to 25 individuals with normal renal function (total of up to 150 individuals) who are scheduled for coronary angiography will be studied. Each individual will have serial measurements of RBF; at baseline, after volume expansion with normal saline, and after exposure to ICM, using the novel technique of contrast enhanced ultrasound (CEU). The investigators will investigate the utility of monitoring RBF with CEU in predicting the occurrence of CN (a rise of > 0.3 mg/dL or 25% in baseline serum creatinine 48 hours after exposure to ICM) after adjusting for other known risk factors in the group of subjects with reduced GFR. The investigators will also examine the correlation between RBF changes and other urinary and serum biomarkers of kidney injury in this group. Up to 25 individuals with a normal kidney function will be studied in a separate part of the study in which the accuracy of CEU based measurements of RBF will be compared to the RBF and blood flow velocity obtained simultaneously using a Doppler flow probe placed directly inside the main renal artery during coronary angiogram procedure. Total to enroll = 150.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for albumin iodinated i-131 serum

Condition Name

Condition Name for albumin iodinated i-131 serum
Intervention Trials
Systemic Exertion Intolerance Disease (SEID) 1
Type 2 Diabetes Mellitus 1
Chronic Fatigue Syndrome 1
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Condition MeSH

Condition MeSH for albumin iodinated i-131 serum
Intervention Trials
Overweight 1
Orthostatic Intolerance 1
Diabetes Mellitus, Type 2 1
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Clinical Trial Locations for albumin iodinated i-131 serum

Trials by Country

Trials by Country for albumin iodinated i-131 serum
Location Trials
United States 2
India 1
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Trials by US State

Trials by US State for albumin iodinated i-131 serum
Location Trials
New York 1
Virginia 1
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Clinical Trial Progress for albumin iodinated i-131 serum

Clinical Trial Phase

Clinical Trial Phase for albumin iodinated i-131 serum
Clinical Trial Phase Trials
Phase 1 1
N/A 2
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Clinical Trial Status

Clinical Trial Status for albumin iodinated i-131 serum
Clinical Trial Phase Trials
Completed 1
Unknown status 1
Active, not recruiting 1
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Clinical Trial Sponsors for albumin iodinated i-131 serum

Sponsor Name

Sponsor Name for albumin iodinated i-131 serum
Sponsor Trials
Era's Lucknow Medical College 1
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) 1
University of Virginia 1
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Sponsor Type

Sponsor Type for albumin iodinated i-131 serum
Sponsor Trials
Other 3
NIH 3
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