Demedetomidine and Remifentanil in Electroconvulsive Therapy (ECT)
Sponsor: Inonu University • ClinicalTrials.gov ID: NCT07824817
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Electroconvulsive therapy (ECT) is a treatment modality that induces therapeutic seizures through electrical stimulation for the management of certain psychiatric disorders. Nearly all ECT procedures are performed under general anesthesia. However, ECT is commonly associated with acute hyperdynamic responses immediately following electrical stimulation, including transient hypertension and tachycardia. These acute hemodynamic changes may pose significant risks, particularly in patients with ischemic heart disease, hypertension, or cerebrovascular disease. Therefore, the hemodynamic response, seizure quality, and recovery profile are critical factors influencing the choice of anesthetic and adjuvant agents. The primary goal of anesthesia for ECT is to maintain hemodynamic stability without compromising seizure duration or quality while ensuring rapid and safe recovery
Interventions
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Saline (0.9% NaCl)
(Drug)
Saline will infused over 10 minutes (total volume: 30 mL)
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Dexmedetomidine
(Drug)
Dexmedetomidine at a dose of 0.5 μg/kg will infused over 10 minutes (total volume: 30 mL)
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Remifentanil
(Drug)
Remifentanil at a dose of 1 μg/kg will infused over 10 minutes (total 30 ml)
Eligibility criteria
Conditions
Locations
- Inonu Universitesi Turgut Ozal Tıp Merkezi — Malatya, Battalgazi, Turkey (Türkiye)
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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