Stellate Ganglion Block Combined With Dexmedetomidine or Subanesthetic Ketamine Infusion for Treatment of Neurostorm.

Study Purpose

Neurostorming is a sudden and exaggerated stress response as a result of damage to the brain. With appropriate treatment and time, there is hope for individuals to overcome storming, regain consciousness, and work towards successfully recovering from brain injury. Most treatments for neurostorming involve the use of medications only such as dexmedetomidine, opioids, gabapentin and propofol to address secondary complications like high blood pressure and fever. These medications focus on slowing the body's stress response or relaxing the body. Stellate ganglion block (SGB) is a promising therapy for paroxysmal sympathetic hyperactivity (PSH), overcoming the limitations of systemic medications and may serve to recalibrate aberrant autonomic states. Ketamine is a potent dissociative agent which has sedative, analgesic and anesthetic properties beside its sympathomimetic effect. Its combination with stellate ganglion block is to oppose its sympathomimetic effect. Dexmedetomidine has analgesic and sedative effect which inhibits the sympathetic nerve activity through its action on the α2 receptor in the spinal cord. Hypothesis: Null hypothesis: There is no difference between the effects of stellate ganglion block combined with dexmedetomidine or subanesthetic ketamine infusion for treatment of neurostorm after traumatic brain injury in critically ill patients.Alternative hypothesis: There is a difference between the effects of stellate ganglion block combined with dexmedetomidine or subanesthetic ketamine infusion for treatment of neurostorm after traumatic brain injury in critically ill patients.which has sedative, analgesic and anesthetic properties beside its sympathomimetic effect. Aim of the work is achievement of effective treatment for the neurostorm after traumatic brain injury in critically ill patients with better outcomes and decrease intensive care unit (ICU) stay.

Recruitment Criteria

Accepts Healthy Volunteers Healthy volunteers are participants who do not have a disease or condition, or related conditions or symptoms	No
Study Type An interventional clinical study is where participants are assigned to receive one or more interventions (or no intervention) so that researchers can evaluate the effects of the interventions on biomedical or health-related outcomes. An observational clinical study is where participants identified as belonging to study groups are assessed for biomedical or health outcomes. Searching Both is inclusive of interventional and observational studies.	Interventional
Eligible Ages	18 Years and Over
Gender	All

More Inclusion & Exclusion Criteria

Inclusion Criteria:

1. Written informed consent from 1st degree relative. 2. Physical ASA status I &

II. 3.

BMI less than or equal 35. 4. Traumatic brain injury patients. 5. Age: ≥18 years old. 6. Sex: both sexes. 7. Paroxysmal sympathetic hyperactivity will be diagnosed on the basis of diagnostic criteria proposed by Blackman et al.(2), The signs of PAID syndrome include:

(1) Severe brain injury (Rancho Los Amigos level IV), (2) temperature of at least 38.5°C, (3) pulse of at least 130 beats/min, (4) respiratory rate of at least 140 breaths/min, (5) agitation, (6) diaphoresis, and (7) dystonia (i.e. rigidity or decerebrate posturing).

The duration is at least 1 cycle/day for at least 3 days.

Exclusion Criteria:

- 1) Known hypersensitivity to study drugs.

2) Patients with primary brain stem injury or brain stem hemorrhage 3) Severe systemic organ diseases. 4) GCS score =3 points 5) Patients complicated with severe coagulation abnormalities, hemorrhagic shock, multiple organ failure. 6) Patients with a history of cerebral hemorrhage or cerebral infarction within the past 3 months. 7) Patients complicated with a history of end stage malignancy. 8) Patients complicated with a history of uncontrolled epilepsy.

Trial Details

Trial ID: This trial id was obtained from ClinicalTrials.gov, a service of the U.S. National Institutes of Health, providing information on publicly and privately supported clinical studies of human participants with locations in all 50 States and in 196 countries.	NCT06354673
Phase Phase 1: Studies that emphasize safety and how the drug is metabolized and excreted in humans. Phase 2: Studies that gather preliminary data on effectiveness (whether the drug works in people who have a certain disease or condition) and additional safety data. Phase 3: Studies that gather more information about safety and effectiveness by studying different populations and different dosages and by using the drug in combination with other drugs. Phase 4: Studies occurring after FDA has approved a drug for marketing, efficacy, or optimal use.	N/A
Lead Sponsor The sponsor is the organization or person who oversees the clinical study and is responsible for analyzing the study data.	Zagazig University
Principal Investigator The person who is responsible for the scientific and technical direction of the entire clinical study.	Eslam S. Almaghawry Mohamed, MD
Principal Investigator Affiliation	Zagazig University
Agency Class Category of organization(s) involved as sponsor (and collaborator) supporting the trial.	Other
Overall Status	Enrolling by invitation
Countries	Egypt
Conditions The disease, disorder, syndrome, illness, or injury that is being studied.	Paroxysmal Sympathetic Hyperactivity

Additional Details

PATIENTS AND METHODS.I. Technical Design: 1. Site of study: This study will be carried out in the emergency intensive Care unit (ICU) of Zagazig University Hospitals within 6 months. 2. Sample size: The sample size was collected using G power version 3.1.9.7 according to the following expected moderate effect size between stellate ganglion plus dexmedetomidine group (SD group) and stellate ganglion block plus ketamine group (SK group) (d=0.5) CI 95% and power 80% the sample size was calculated to be 102,51 in each group. 3. Patients included in this study:

- Inclusion criteria: 1.

Written informed consent from 1st degree relative. 2. Physical ASA status I &

II. 3.

(1) Severe brain injury (Rancho Los Amigos level IV), (2) temperature of at least 38.5°C, (3) pulse of at least 130 beats/min, (4) respiratory rate of at least 140 breaths/min, (5) agitation, (6) diaphoresis, and (7) dystonia (i.e. rigidity or decerebrate posturing).

The duration is at least1 cycle/day for at least 3 days.

- Exclusion criteria: 1.

Known hypersensitivity to study drugs. 2. Patients with primary brain stem injury or brain stem hemorrhage. 3. Severe systemic organ diseases. 4. GCS score =3 points. 5. Patients complicated with severe coagulation abnormalities, hemorrhagic shock, multiple organ failure. 6. Patients with a history of cerebral hemorrhage or cerebral infarction within the past three months. 7. Patients complicated with a history of end stage malignancy. 8. Patients complicated with a history of uncontrolled epilepsy. Withdrawal criteria: The patient has the right to withdraw from the study at any time without any negative consequence on their medical treatment plan.

II. Operational Design: 1.

Type of study: Double-blinded randomized clinical trial. 2. Parameters of the study will include: All patients suspected of having PSH will underwent detailed clinical history and physical examination. Hemodynamics monitoring including heart rate and mean arterial pressure (MAP) also temperature monitoring will be done as base line before the block and after stellate ganglion block every one hour over 24 hours until remission (till return to normal values for age and sex). These patients will be also subjected to routine hematological investigations including, complete blood count, kidney and liver function test, coagulation profile, urine analysis for myoglobinuria and thyroid profile. septic screening including, blood, urine, tracheal aspirate and sputum culture and radiological assessment by using chest x-ray. All patients developing PSH will be randomly allocated by using computerized generated randomization table into two groups: SD group: Stellate ganglion block and 1 ug/kg/h intravenous Dexmedetomidine infusion. SK group: Stellate ganglion block and 0.5 mg/kg/h intravenous ketamine infusion. Stellate ganglion block : Patients will undergo an ultrasonography-guided SGB at bedside under standard American Society of Anesthesiologists monitoring standards. The patient will be placed in supine position with the head turn to the opposite side. The anterior and lateral parts of the neck will be prepped with chlorhexidine, and a linear (13-6 MHz) ultrasound probe will be applied to the anterolateral neck at the cricoid cartilage level to identify the transverse process of C6 and C7, anterior tubercle of C6 (Chassaignac tubercle), longus colli muscle and surrounding neurovascular structure. The needle will be advanced with an in-plane technique and aimed to deposit the local anesthetics medial to the Chassaignac tubercle and anterior to pre-vertebral fascia of longus colli muscle. After that, a catheter will be advanced through the needle and secured in place. After aspiration, 10 ml of bupivacaine 0.25% solution will be injected through the catheter and repeated every 48 hours till time of remission. a. Data to be measured: 1. Demographic data including, age, sex, BMI, ASA classification. 2. Hemodynamics including, MAP and heart rate and temperature measurement as base line before stellate ganglion block, after stellate ganglion block and furtherly every hour over 24 hours till time of remission (return to normal value for age and sex). 3. Remission time of paroxysmal hypertension (min): time from the start of treatment till return to normal blood pressure). 4. Remission time of paroxysmal tachycardia (min): time from the start of treatment till return to normal heart rate). 5. Remission time of paroxysmal hypermyotonia (day): the criteria of muscle hyperactivity is the rigid posture or sever dystonia (i.e. rigidity or decerebrate posturing). 6. Remission time of decrease respiratory rate below 25 breath/min (min): time from the start of treatment till time of decrease respiratory rate below 25 breath/min. 7. Changes in glascow coma scale score (GSC) from admission to ICU till discharge: GSC will be evaluated once daily. 8. Duration of ICU stay (days): the duration from the admission till discharge from ICU.

Arms & Interventions

Arms

Experimental: SD group

Stellate ganglion block and 1 ug/kg/h intravenous Dexmedetomidine infusion

Experimental: SK group

Stellate ganglion block and 0.5 mg/kg/h intravenous ketamine infusion.

Interventions

Procedure: - Stellate ganglion block

Sympathectomy by using combination of regional nerve block and systemic drugs

Drug: - Dexmedetomidine

intravenous Dexmedetomidine infusion

Drug: - Ketamine

intravenous ketamine infusion

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International Sites

Zagazig university, Zagazig, Egypt

Status

Address

Zagazig university

Zagazig, ,

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