Viewing Study NCT06554886



Ignite Creation Date: 2024-10-26 @ 3:37 PM
Last Modification Date: 2024-10-26 @ 3:37 PM
Study NCT ID: NCT06554886
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-06-24

Brief Title: A Study Investigating Peripheral Cryoneurolysis in Adults With Chronic Migraine
Sponsor: None
Organization: None

Study Overview

Official Title: An Open Label Pilot Study Investigating the Safety and Efficacy of a Percutaneous Peripheral Cryoneurolysis Therapy in Medically Resistant Chronic Migraine
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The trial is a research study that tests a freezing technique called cryoneurolysis to see if it helps relieve pain in adults with chronic migraine Chronic migraine is a condition that causes moderate to severe headache

In this study the investigators want to evaluate the freezing technique in chronic migraine The main goal is to see how much headache relief is experienced after receiving the treatment The investigators will also record other important information about the participants

The study is looking to recruit 12 adults with chronic migraine to take part in the study Participants will register their headache burden in a headache diary for at least 4 weeks before receiving treatment with the freezing technique They will continue to register headache in the headache diary during the follow-up After this initial treatment participants with recurring headache can receive treatment as needed for up to two years

The results of this study will help us decide if the freezing technique may be viable treatment option for chronic migraine and enable us plan for further studies on this treatment
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None