Frailty Clinical Trial - The Effects of Frailty on Opioid Consumption

Status Not yet recruiting

Clinical Trial Summary

The FRAIL scale will be applied to patients at the preoperative visit. According to the FRAIL Scale, patients will be divided into 3 groups as Non-frail (Group I), pre-frail (Group II) and frail (Group III). After routine preoperative preparation and monitoring, patients will be given spinal anesthesia. Demographic data and intraoperative data of the patients will be recorded. Patients will be transferred to the post-operational post-operative care unit (PACU) and patient-controlled analgesia (PCA) will be applied to each patient with a standard protocol. In the postoperative period, the need for analgesics will be recorded for 24 hours, and if additional analgesics are needed, they will be recorded. Pain scores of the patients will be evaluated for 24 hours.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05445700
Study type	Interventional
Source	Selcuk University
Contact	Mehmet SARGIN, Associate Professor
Phone	+90 (332) 241 50 00
Email	mehmet21sargin@yahoo.com
Status	Not yet recruiting
Phase	N/A
Start date	July 15, 2022
Completion date	September 15, 2022

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