DRUG
Midodrine Oral Tablet
midodrine group will receive midodrine 10 mg PO q 8 hr with gradual weaning of IV nor-adrenaline after receiving 4 doses of oral midodrine .
Status
Unknown
Phase
Phase 2
Enrollment
90
Locations
1
Results
Not posted
Publications
0
Study summary
the study is developed to evaluate the effect of use of oral vasopressors (midodrine versus minirin) on weaning ICU patients from IV vasopressors (noradrenaline) and compare between them for efficacy in shortage the duration of IV vasopressor and has low complications and side effects.
Interventions
DRUG
midodrine group will receive midodrine 10 mg PO q 8 hr with gradual weaning of IV nor-adrenaline after receiving 4 doses of oral midodrine .
DRUG
Minirin group will receive minirin 60 µg PO q 8 hr with gradual weaning of IV nor-adrenaline after receiving 4 doses of oral minirin .
DRUG
control group will receive IV nor-adrenaline and is gradually weaning from it according to routine hospital care without adding oral midodrine or oral minirin .
Timeline
First posted
Oct 14, 2020
Study start
Oct 15, 2020
Primary completion
Jan 1, 2021
Study completion
Jan 28, 2021
Results posted
Not reported
Registry updated
Oct 14, 2020
Outcomes
liberation the patient from IV vasopressors with maintaining hemodynamics.
Time frame · 48 hrs
Blood pressure will be assessed regularly every 15 minutes
Not reported in the indexed record.
Eligibility
Inclusion Criteria: * Age of 18 - 60 years. * Patients of both genders. * Patients diagnosed by spinal shock and they are in the recovery stage . Exclusion Criteria: * Patient refusal. * Anuric or oliguric patients or patients with chronic kidney disease. * Patients with allergy to medication included in the study.
Study locations
Egypt. Showing up to 24 locations stored in the fast local snapshot.
Ahmed Talaat Ahmed
Asyut, Egypt
Publications
No PMID-linked publications were present in this registry snapshot.
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