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NCT07139847
Magnesium Sulfate for Prevention of Emergence Agitation in Lumbar Disc Surgery
Conditions: Lumbar Disc Herniation, Emergence Agitation, Magnesium Sulfate
Sex: All
Ages: 18 Years – 70 Years
Healthy volunteers: No
Enrollment: 70
Sponsor: Ondokuz Mayıs University
Summary
In this retrospective study, the effect of intraoperative magnesium sulfate infusion on the incidence of postoperative emergence agitation was evaluated in adult patients who underwent elective lumbar microdiscectomy under general anesthesia. The medical records of patients aged 18-70 years with an ASA physical status of I-II were retrospectively reviewed. Patients were evaluated according to whether they received intraoperative magnesium sulfate infusion as part of anesthetic management. The primary outcome measure was the incidence of emergence agitation in the post-anesthesia care unit; this assessment was based on Ramsay Sedation Scale scores recorded in the post-anesthesia care unit at admission and at 5, 10, 15, and 30 minutes. Secondary outcome measures included postoperative pain scores assessed using the Numeric Rating Scale, intraoperative remifentanil consumption, recovery and extubation times, tramadol requirement in the post-anesthesia care unit, and possible adverse events related to magnesium infusion.
Eligibility Criteria
Inclusion Criteria:
Age between 18 and 70 years
ASA physical status classification I or II
Scheduled for elective single-level lumbar microdiscectomy under general anesthesia
Ability to provide written informed consent
Exclusion Criteria:
Severe cardiovascular disease
History of psychiatric disorder
Neuromuscular disease
Pregnancy or breastfeeding
Hepatic or renal dysfunction
Current use of calcium channel blockers, hypnotics, anxiolytics, or antipsychotic medications
Known allergy to magnesium sulfate or study-related medications
Refusal to participate in the study
Source: ClinicalTrials.gov (NCT07139847). StuddyBuddy aggregates publicly available trial information.