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Clinical Trial Summary

In this study, the investigators aim to reduce complications in orthopedic malignancy surgeries and to increase the quality of life of patients who will be operated on.


Clinical Trial Description

In the preoperative period, the participants will be taken to the block room. The participants will be monitored, standard sedation will be applied. Patients in the first group will be provided with preoperative and peroperative analgesia with an epidural catheter. The second group patient will be get no block. Afterwards, both groups will be operated under similar general anesthesia conditions. A patient-controlled analgesia device will be attached to each group of participants and their postoperative follow-up will be made. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04945512
Study type Interventional
Source Istanbul University
Contact Nur Canbolat, MD
Phone +905325162583
Email drnurekiz@gmail.com
Status Recruiting
Phase N/A
Start date November 7, 2021
Completion date September 20, 2022

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