CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 134 enrolled
Drug / intervention
urological surgical interventionprocedure
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06232980
NCT06232980N/ACompleted
CompareCT.gov

Evaluation of Observer Alertness/Sedation Score (OAA/S) and Bispectral Index (BIS) Parameters for Induction of General Anesthesia With Propofol in Geriatric Patients

Ankara City Hospital Bilkent·interventional·Posted Jan 31, 2024·Updated Oct 26, 2024

In Brief

A clinical study evaluating urological surgical intervention for E03.155.253 and 2 related conditions. Completed, enrolled 134 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsE03.155.253, Bispectral Index Monitor, Hypotension
CountriesTurkey (Türkiye)
Collaborators--

Timeline

N/ACompletedFinished
202420252026
First PostedJan 31, 2024
Enrollment StartSep 1, 2023
Primary CompletionMar 29, 2024
Study CompletionApr 15, 2024
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 2.4 years ago

Interventions

urological surgical interventionprocedure

Anesthesia induction will be performed with propofol, and ventilation will be maintained with a laryngeal mask for urological surgical procedures.