Current partner codePEPTIDESDE
NCT04586790·Phase 2·INTERVENTIONAL

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

Status

Unknown

Phase

Phase 2

Enrollment

90

Locations

1

Results

Not posted

Publications

0

Study summary

What the protocol is testing.

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

Treatment arms and agents.

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 .

DRUG

Minirin oral tablet

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

Nor-Adrenaline

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

From registration to results.

  1. First posted

    Oct 14, 2020

  2. Study start

    Oct 15, 2020

  3. Primary completion

    Jan 1, 2021

  4. Study completion

    Jan 28, 2021

  5. Results posted

    Not reported

  6. Registry updated

    Oct 14, 2020

Outcomes

What the study measures.

Primary outcomes

liberation the patient from IV vasopressors with maintaining hemodynamics.

Time frame · 48 hrs

Blood pressure will be assessed regularly every 15 minutes

Secondary outcomes

Not reported in the indexed record.

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
60 Years
Sex
ALL
Healthy volunteers
No

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

1 registered sites.

Egypt. Showing up to 24 locations stored in the fast local snapshot.

Ahmed Talaat Ahmed

Asyut, Egypt

Publications

Results and literature.

No PMID-linked publications were present in this registry snapshot.

Primary links

Continue at the source.

Related trials

More studies on Desmopressin.

Related PeptideStat pages

Put the record in context.

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