Effect of propofol in severe intracerebral hemorrhage

Phase 3

Recruiting

• Conditions: ontraumatic intracranial hemorrhage.; Nontraumatic intracranial hemorrhage, unspecified; I62.9

• Registration Number: IRCT20200208046414N1
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 April 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 112

Inclusion Criteria

Acute ICH over 15 years of ages
No surgery indication by the neurosurgery team
NIHSS above 15

Exclusion Criteria

Pregnancy &lactation
Concurrent Malignancy
CKD or chronic hepatic failure or another chronic sickness
History of drug sensitivity used in the study

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
IHSS. Timepoint: onset of study . 7th day .90th day. Method of measurement: table of NIHSS.;MRS. Timepoint: Onset of study . 7th and 90th day. Method of measurement: Table of MRS.;Brain Edema. Timepoint: 3th & 7th day. Method of measurement: Brain CT scan.;Expansion of Hemorage. Timepoint: 3th &7th day. Method of measurement: Brain CT scan.

Secondary Outcome Measures

Name	Time	Method
Time of Hospitalization. Timepoint: End of hospitalization. Method of measurement: day.;Mortality rate. Timepoint: mortality. Method of measurement: yes /no.;Time of intubation. Timepoint: End of Intubation. Method of measurement: day.;Complication. Timepoint: End of study. Method of measurement: Brain CT.