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Mgso4 as Neuroprotective in Post Traumatic Brain Injury

Primary Purpose

Magnesium Sulphate, Traumatic Brain Injury, Brain

Status
Completed
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
Magnesium Sulfate
Placebo
Sponsored by
Osama Mohamed Abdelwahab
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Magnesium Sulphate focused on measuring Magnesium, Sulphate, double, blinded, randomized, control, study

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1) Patients with moderate (GCS = 9-12), or severe (GCS = 3-8) traumatic brain injury.

    2) Age above 12 years.

    3) Consenting for treatment within 24 hours of trauma.

Exclusion Criteria:

  • 1) Non consenting patients.

    2) Persistent hypotension (BP below 90 / 60) in 1st 24 hours despite measures of resuscitation.

    3) Significant multisystem association (e.g. cord injury with spinal shock).

    4) Known case of renal failure

Sites / Locations

  • Faculty of medicine , Cairo university

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

intervention arm ( Group A )

Placebo arm (Group B )

Arm Description

including 30 patients Group A was given magnesium Sulphate Administration regimen of Mgso4 was as following: Initial dose: within 24 hrs of trauma 50 mg / kg / IV infusion over 1 hour. Maintenance dose: (25 mg / kg) per dose twice daily for 48 hrs.

including 30 patients Placebo control study Group B was given saline as a placebo. with the same regimen and route of administration of magnesium sulphate

Outcomes

Primary Outcome Measures

Glasgow outcome scale after 2 months
assessment of conscious level of the patients after 60 days of drug administration The Glasgow outcome scale (GOS) has been used to categorize the outcome after 2 months as follows: Death. Persistent vegetative state: Minimal responsiveness. Severe disability: Conscious but disabled; dependent on others for daily support. Moderate disability: Disabled but independent; can work in sheltered setting. Good recovery: Resumption of normal life despite minor deficits. Better score means that the patient conscious level is improved

Secondary Outcome Measures

Full Information

First Posted
February 22, 2020
Last Updated
November 20, 2020
Sponsor
Osama Mohamed Abdelwahab
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1. Study Identification

Unique Protocol Identification Number
NCT04646876
Brief Title
Mgso4 as Neuroprotective in Post Traumatic Brain Injury
Official Title
Assessment Role of Mgso4 as Neuroprotective in Post Traumatic Brain Injury
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
May 2, 2019 (Actual)
Primary Completion Date
March 12, 2020 (Actual)
Study Completion Date
June 2, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Osama Mohamed Abdelwahab

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to assess the potential role of magnesium sulphate (MgSo4) as a neuroprotective agent using the Glasgow outcome scale following moderate and severe traumatic brain injury.
Detailed Description
The study is Prospective , Comparative , double-blind , placebo-controlled study with randomization Patients with post traumatic brain injury either moderate (glasgow coma scale GCS = 9-12) or severe (GCS = 3-8) admitted in one of the neurosurgical ICU of the following centers; kasr El Aini Hospitals, Beni- Suef University Hospital or Beni- Suef General Hospital. Study design and statistical inferences Patients with traumatic brain injury included in the study will be randomly allocated into one of two equal groups (30 patients each): - Group (A): will receive MgSo4. Group (B): will receive normal saline as a placebo. Each patient will receive all other standard management as indicated on individual basis (e.g. Antiepileptics, brain dehydrating measures, antibiotics, ventilatory support, or surgical intervention when deemed necessary). The Glasgow outcome scale (GOS) will be used to categorize the outcome after 2 months as follows: Death Persistent vegetative state: Minimal responsiveness Severe disability: Conscious but disabled; dependent on others for daily support Moderate disability: Disabled but independent; can work in sheltered setting Good recovery: Resumption of normal life despite minor deficits For each patient, the following will be recorded: Personal data: name, age, sex, address, tel. No. Mode of trauma: fall from height, road traffic accidents, or isolated head trauma. Neurological assessment on admission using the Glasgow coma score. Associated injuries or neurological deficits. Findings of initial CT brain, as well as follow up scans. Any previous illness. Administration : Administration regimen of Mgso4 will be as following: Initial dose: within 24 hrs of trauma 50 mg / kg / IV infusion over 1 hour. Maintenance dose: 25 mg / kg twice daily for 48 hrs. In order to avoid Mgso4 toxicity, infusion of the medication (either Mgso4 or placebo) will be abruptly terminated whenever: Urine output < 0.5 ml / kg / hour over 4 hours Blood urea > 50 mg/ dL . Fall of systolic BP < 90 mm Hg. Respiratory center depression (respiratory rate less than 12 per minute). Cardiac arrhythmia. Loss of deep tendon reflexes. The third supervisor will be responsible for the safety measures of the study, which will be evaluated by continuous monitoring of vital signs, arterial blood pressure (systolic, diastolic), urine output, serum chemistry. Preparation of the drug: The medication will be prepared by three assistants other than the researcher, one in each center where the study will be conducted. For each patient, a set of bottles will be prepared (initial dose, and 4 maintenance doses). After preparation, each set of bottles will be labeled using the same code consisting of letters (A, B, C, D, E, F) and figures (0 to 9). Total number of codes will be 60 which is the total number of patients allocated (A0, A1, A2,....A9& B0, B1, ......B9& C1,...C9& D0-D9&E0-E9& F0-F9). Only the second supervisor will be acquainted with the key of the code, either it is the studied treatment (Mg So4), or normal saline (placebo). He will be responsible for the random allocation of the patients, and instructing the assistants to prepare either the treatment or the placebo, and their subsequent coding. He will not be informed about the results which will be regularly followed by the first supervisor. The key will be kept hidden from the researcher who will be responsible for recording the results. The key will be disclosed only after conclusion of the study and collecting the results in order to operate the statistical analysis. Each amp of Mgso4 (0.5 gm / 5ml) will be dissolved in 13.5 ml normal saline (at that concentration, Mgso4 will remain chemically stable for 3 months in room air). For simplicity, this will compose a unit and will be labeled as mentioned. So one unit equals 500 mg dissolved in 13.5 ml normal saline. For each patient, the number of units will be calculated according to the body weight. For example, the initial dose or the daily dose of 70 kg patient equals 7 units (70 x 50 = 3500 mg). For this patient, 3 bottles will be prepared on admission, each bottle will be labeled the same as the units, and each bottle will contain 7 units. The first bottle will be given as the initial dose, and the other two bottles will be divided to 4 equal doses, and will be given over the next 48 hrs. For placebo, the same will be done, but only using normal saline. Which is identical to Mgso4 regarding color and aspect.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Magnesium Sulphate, Traumatic Brain Injury, Brain, Injury
Keywords
Magnesium, Sulphate, double, blinded, randomized, control, study

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
2 groups, comparative
Masking
ParticipantCare ProviderOutcomes Assessor
Masking Description
The researcher did not know the type of medication given to the patients, placebo or treatment actually Only investigator knew the key
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
intervention arm ( Group A )
Arm Type
Active Comparator
Arm Description
including 30 patients Group A was given magnesium Sulphate Administration regimen of Mgso4 was as following: Initial dose: within 24 hrs of trauma 50 mg / kg / IV infusion over 1 hour. Maintenance dose: (25 mg / kg) per dose twice daily for 48 hrs.
Arm Title
Placebo arm (Group B )
Arm Type
Placebo Comparator
Arm Description
including 30 patients Placebo control study Group B was given saline as a placebo. with the same regimen and route of administration of magnesium sulphate
Intervention Type
Drug
Intervention Name(s)
Magnesium Sulfate
Other Intervention Name(s)
Mgso4
Intervention Description
Prospective , comparative , double blind study
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Saline
Intervention Description
Prospective , comparative , double blind study
Primary Outcome Measure Information:
Title
Glasgow outcome scale after 2 months
Description
assessment of conscious level of the patients after 60 days of drug administration The Glasgow outcome scale (GOS) has been used to categorize the outcome after 2 months as follows: Death. Persistent vegetative state: Minimal responsiveness. Severe disability: Conscious but disabled; dependent on others for daily support. Moderate disability: Disabled but independent; can work in sheltered setting. Good recovery: Resumption of normal life despite minor deficits. Better score means that the patient conscious level is improved
Time Frame
60 days from drug administration

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1) Patients with moderate (GCS = 9-12), or severe (GCS = 3-8) traumatic brain injury. 2) Age above 12 years. 3) Consenting for treatment within 24 hours of trauma. Exclusion Criteria: 1) Non consenting patients. 2) Persistent hypotension (BP below 90 / 60) in 1st 24 hours despite measures of resuscitation. 3) Significant multisystem association (e.g. cord injury with spinal shock). 4) Known case of renal failure
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Osama Awahab, professor
Organizational Affiliation
Faculty Of Medicine , Beni Suef University , Egypt
Official's Role
Principal Investigator
Facility Information:
Facility Name
Faculty of medicine , Cairo university
City
Cairo
ZIP/Postal Code
11511
Country
Egypt

12. IPD Sharing Statement

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Mgso4 as Neuroprotective in Post Traumatic Brain Injury

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