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Evaluation of T2, T3 Sympathectomy for Postmastectomy Pain Syndrome by Pulse Oximeter

Analgesia Clinical Trial

Official title:
Evaluation of T2, T3 Sympathectomy for Postmastectomy Pain Syndrome by Thermal Radiofrequency Versus Chemical Neurolysis Using Perfusion Index Derived Pulse Oximeter

Clinical Trial Summary

The aim of the study is to compare the efficacy of T2, T3 sympathetic block using thermal radiofrequency versus chemical neurolysis in postmastectomy pain syndrome using perfusion index derived from pulse oximetry.

Clinical Trial Description

Postmastectomy pain is a chronic pain condition with neuropathic nature. Several drugs and methods are used for its management. This study was designed to compare the efficacy of both thermal radiofrequency and chemical neurolysis in management of postmastectomy pain through using perfusion index derived from pulse oximetry. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04953507
Study type Interventional
Source National Cancer Institute, Egypt
Contact Walaa Y Elsabeeny, MD
Phone 01007798466
Email walaa.elsabeeny@nci.cu.edu.eg
Status Recruiting
Phase N/A
Start date July 3, 2021
Completion date December 2024
View Details
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