A Prospective Study of Different Digoxin Treatment Regimens in Egyptian Hospital
NCT ID: NCT02489786
Last Updated: 2015-07-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
71 participants
INTERVENTIONAL
2012-10-31
2014-10-31
Brief Summary
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Objective: To evaluate and compare the digoxin serum concentration and patient's quality of life in the continuous versus interrupted digoxin dosing regimens.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Regimen 1
patient takes 0.25mg of digoxin daily except friday
patients take 0.25 mg of digoxin daily except friday
Regimen 2
patient takes 0.25mg of digoxin daily except Thursday and Friday
patients take 0.25 mg of digoxin daily except thursday and friday
Regimen 3
patient takes 0.125mg of digoxin daily
patients take 0.125 mg of digoxin daily
Regimen 4
digoxin dose is calculated using Jusko-Koup method and given daily
digoxin dose is calculated using Jusko-Koup method and given daily
Interventions
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patients take 0.25 mg of digoxin daily except friday
patients take 0.25 mg of digoxin daily except thursday and friday
patients take 0.125 mg of digoxin daily
digoxin dose is calculated using Jusko-Koup method and given daily
Eligibility Criteria
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Inclusion Criteria
* with or without congestive heart failure (CHF)
* taking digoxin tablets with or without holiday regimens
Exclusion Criteria
* diagnosed with thyroid disorders (hyperthyroidism \& hypothyroidism).
* diagnosed with renal failure
* pregnant
18 Years
70 Years
ALL
No
Sponsors
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Cairo University
OTHER
Responsible Party
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Sahar Atef ALShabasy
Teaching Assistant
Other Identifiers
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CL (312)
Identifier Type: -
Identifier Source: org_study_id
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