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Occipital Nerve RF Between Occipital Nerve Block And Occipital Nerve Radiofrequency Ablation

Headache Clinical Trial

Official title:
A Comparison of Pain Control AND Quality of Life Improvement Between Occipital Nerve Block And Occipital Nerve Radiofrequency Ablation: A Double-Blind Single Center Prospective Study

Clinical Trial Summary

This is a randomized, double blind, single-center, clinical trial. The study will be conducted over a period of 6 months. The study will be conducted at the Allevio Pain Clinic, Toronto, Canada.

Clinical Trial Description

During the first visit the investigator will assess potential subject's eligibility. Screening and recruitment, and randomization, and administer questionnaires will be performed by research coordinator. Study informed consent form (ICF) can be signed on the RF procedure day. If additional visits will be required to finalize the procedures related to the first visit they will be scheduled accordingly. After randomization the qualified participants will be scheduled for their bilateral Occipital RF or bilateral Occipital Block. Participants will be asked to complete the follow-up questionnaires at baseline, 3 and 6 months. On their last study visit, participants will have an exit interview, in addition to completing study measures. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04124458
Study type Interventional
Source Allevio Pain Management Clinic
Contact SHADI BABAZADEH, MD
Phone +16474788462
Email Shadi.Babazadeh@AllevioClinic.com
Status Not yet recruiting
Phase N/A
Start date January 2, 2023
Completion date December 31, 2025
View Details
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