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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05610774
Other study ID # RC 23.9.2022
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 20, 2022
Est. completion date December 20, 2023

Study information

Verified date July 2023
Source Benha University
Contact Samar R Amin, MD
Phone 01287793991
Email samar.rafik@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dexmedetomidine was reported to effectively reduce cerebral metabolism and ICP by decreasing cerebrospinal fluid pressure in patients with cerebral tumors or head injuries that require craniotomy. However, it was also reported to exhibit no effect on ICP. the effect of MgSO4 associated with dexmedetomidine on ONSD in severely pre-eclamptic parturient has been understudied . Though this study aims to evaluate the effect of dexmedetomidine infusion on raised ICP in severely pre-eclamptic parturients using ocular ultrasonography to determine ONSD as a measure of ICP.


Description:

Dexmedetomidine, a highly selective α-2-receptor agonist, is a first-line sedative medication in ICU and has been increasingly used for obstetric anesthesia. Dexmedetomidine, which provides light sedation, possesses analgesic, sympatholytic, anxiolytic properties and attenuates the stress response without significant respiratory depression. In addition, dexmedetomidine-induced stimulation of postsynaptic alpha-2 adrenergic receptor on the cerebral blood vessels can cause cerebral vasoconstriction and decrease cerebral blood flow. However, the effects of dexmedetomidine on ICP are controversial. Clinical signs of raised ICP are not specific and often difficult to interpret, especially during pregnancy and pre-eclampsia. Though the use of invasive devices is considered a gold standard in the measurement of ICP, Ocular sonography is a promising bedside tool, which serves as a noninvasive, readily available, and cost-effective means for indirectly measuring ICP. Bedside ultrasound can be used as a point-of-care tool for rapidly measuring the optic nerve sheath diameter (ONSD), which is a validated indirect means for measuring ICP. An increase in ICP reflects as a raised ONSD since the optic nerve is surrounded by Dural sheath and cerebrospinal fluid (CSF) containing subarachnoid space, which is distensible in the retrobulbar segment, particularly when CSF pressures rise.


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date December 20, 2023
Est. primary completion date November 10, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: - aged18 to 40 years with - at least 36 weeks gestation - admitted with diagnosis of severe pre-eclampsia and scheduled to receive Magnesium Sulphate therapy before delivery Exclusion Criteria: - Presence of ocular wound or Prior ocular surgery - emergency cases, and evidence of fetal compromise - HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet levels) - Chronic hypertension - Hyperthyroidism, and diabetes mellitus - Presence of pre-existing chronic lung and/or cardiac diseases - Presence of pre-existing chronic renal and/or hepatic diseases - Presence of any chronic diseases of central nervous system. - known allergies to the tested drug.

Study Design


Intervention

Drug:
Dexmedetomidine
pre-eclamptic Patients will receive a loading dose of iv dexmedetomidine (0.5 ug/kg) diluted in 50 ml saline and given over 10 min, followed by a maintenance infusion of (0.2 ug/kg/h) diluted in 200 ml saline till The sedation scores on the Richmond Agitation and Sedation Scale was -2 to +1 (lightly sedated to restless).
Saline
pre-eclamptic patients will receive 50 ml saline loading for 10 min followed by 200 ml saline infusion

Locations

Country Name City State
Egypt Samar Rafik Amin Banha Qalubia

Sponsors (1)

Lead Sponsor Collaborator
Benha University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Optic nerve sheath diameter (ONSD) measurments following Drug administration Baseline (before starting MgSO4 therapy) then at 1, 6, 12 and 24 hours postoperative
Secondary The incidence of raised ICP in severe pre-eclampsia ONSD >5.0 mm Baseline (before starting MgSO4 therapy), and during 24 hours postoperative.
Secondary Sedation Score the Richmond Agitation and Sedation Scale (RASS), on which scores range from -5 [unresponsive] to +4 [combative]. every 2 hours after drug infusion, till 24 postoperative hours
Secondary Heart Rate (HR) Baseline (before starting MgSO4 therapy) then every 2 hours till 24 postoperative hours
Secondary mean arterial pressure (MAP) changes. Baseline (before starting MgSO4 therapy) then every 2 hours till 24 postoperative hours
Secondary The duration of hospital stay defined as time from the day of operation to the day of discharge one month after delivery
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