CompletedNot Applicable

The Use of Sedation Score and Bispectral Index for Induction in Geriatric Patients

Turkey (Türkiye)134 participantsStarted 2023-09-01

Plain-language summary

The main objective of this clinical study is to determine the effectiveness of BIS-guided propofol administration in avoiding hypotension during propofol induction in geriatric patients. The primary question it aims to answer is whether the mean arterial pressure can be maintained above 60mmHg with BIS-guided propofol induction. For this purpose, the observer's alertness sedation score will be compared with bispectral index-guided inductions.

Who can participate

Age range65 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * T.R. Patients aged 65 and over who will undergo elective surgery under general anesthesia in the Urology Operating Room of the Ministry of Health Ankara City Hospital Exclusion Criteria: * Being under 65 years old * Those who do not have the ability to read, understand and sign the consent form * Hemodynamically unstable patients * Those who have contraindications to anesthetic drugs * Patients who do not want to participate in the study * Patients with advanced dementia * Emergency surgical procedures

What they're measuring

Use of BIS for preventing hypotension (mean arterial pressure (MAP) <60 mmHg) during propofol induction in geriatric patients

Timeframe: The mean arterial pressure (MAP) will be recorded at 2-minute intervals for a duration of 14 minutes.

Trial details

NCT IDNCT06232980

SponsorAnkara City Hospital Bilkent

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-03-29

View on ClinicalTrials.gov More E03.155.253 trials