the Effect of Oral Vasopressors for Liberation From IV Vasopressors in Spinal Shock

Last updated: October 7, 2020
Sponsor: Ahmed talaat ahmed aly
Overall Status: Active - Recruiting

Phase

2

Condition

Low Blood Pressure (Hypotension)

Treatment

N/A

Clinical Study ID

NCT04586790
oral vasopressors
  • Ages 18-60
  • All Genders

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age of 18 - 60 years.

  • Patients of both genders.

  • Patients diagnosed by spinal shock and they are in the recovery stage .

Exclusion

Exclusion Criteria:

  • Patient refusal.

  • Anuric or oliguric patients or patients with chronic kidney disease.

  • Patients with allergy to medication included in the study.

Study Design

Total Participants: 90
Study Start date:
October 15, 2020
Estimated Completion Date:
January 28, 2021

Connect with a study center

  • Ahmed Talaat Ahmed

    Assiut,
    Egypt

    Active - Recruiting

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