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Evaluation of effect of furosemide add on to hypertonic slain on neurohormonal factors in Traumatic brain injury

Evaluation of effect of furosemide add on to hypertonic slain on neurohormonal factors in Traumatic brain injury,A randomized single blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201509283014N10
Enrollment
60
Registered
2016-07-13
Start date
2016-04-18
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

brain injury. Concussion,Traumatic cerebral oedema, Diffuse brain injury, Focal brain injury, Epidural haemorrhage,Traumatic subdural haemorrhage,Traumatic subarachnoid haemorrhage, Intracranial injury with prolonged coma, Other intracranial injuries, Intracranial inju

Interventions

Intervention 1: One groups receives at a dose of 20ml / h and furosemide for 0.05mg / kg / h for 72 hours . Intervention 2: Control group receives for 72 hours at a dose of 20ml /h saline hyperton.
Treatment - Drugs
One groups receives at a dose of 20ml / h and furosemide for 0.05mg / kg / h for 72 hours .
Control group receives for 72 hours at a dose of 20ml /h saline hyperton

Sponsors

Mazandaran University of Medical Sciences, Vice chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: All of patients with 18-90 years old with closed head trauma ; associated with brain edema confirmed with CT scan ; Hemodynamically stable before management; GCS<14; Patients with CV line ; admission with in 24 hours of initial insult

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Bloood Na. Timepoint: 1,2.3.4 days. Method of measurement: Serum concentraion.;Blood osmolality. Timepoint: 1,2,3,4 days. Method of measurement: With calculation of ions affect the osmolarity.

Secondary

MeasureTime frame
??S100B. Timepoint: 1,2,3,4 days. Method of measurement: Kit (spectrophotometery).;NSE. Timepoint: 1,3,5. Method of measurement: Kit (spectrophotometery).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Marziyeh Jafari

Mazandaran University of Medical Sciences

drmjafari1985@yahoo.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026