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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04937010
Other study ID # REB21-0839
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date September 1, 2026

Study information

Verified date July 2023
Source Alberta Health Services, Calgary
Contact Fady Girgis, MD
Phone 4039446497
Email fmgirgis@ucalgary.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to determine the efficacy of occipital nerve stimulation (ONS) in the treatment of chronic trigeminal autonomic cephalalgias (TACs).


Description:

Several open studies and case series have shown improvement in pain scores using ONS specifically for cluster headache, which is the most common of the TACs. However, neuromodulation in the treatment of pain disorders is subject to strong placebo effect and bias, and the lack of controlled studies in this population makes its true efficacy unknown. Therefore, we plan to study ONS in a population of patients with chronic TACs using a double-blind, randomized, controlled, cross-over study. Using sub-threshold stimulation parameters, meaning patients will not know when therapeutic stimulation is active, subjects will rate their pain and quality of life during both therapeutic and sham stimulation periods. Following the cross-over period, all subjects will undergo therapeutic stimulation for 1-year in order to gauge long-term effects.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date September 1, 2026
Est. primary completion date September 1, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Meets ICHD-3 diagnostic criteria for the chronic form of one of the trigeminal autonomic cephalgias (outlined below), as determined by the treating neurologist. - Failed standard medical management, meaning at least 3 conventional preventative therapies. Exclusion Criteria: - Presence of uncontrolled or untreated psychiatric disease - Presence of medical contraindications to surgery - Patient does not consent to surgery - Non-English speaking

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Occipital nerve stimulator implant
Implantation of occipital nerve stimulator and different stimulation parameters

Locations

Country Name City State
Canada University of Calgary Calgary Alberta

Sponsors (1)

Lead Sponsor Collaborator
Alberta Health Services, Calgary

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in headache frequency Change in frequency of headaches 6 months
Secondary Safety of Occipital Nerve Stimulation Any adverse events with stimulation 6 months
See also
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Recruiting NCT04930887 - Clinical Trial of Endoscopically Guided Injection of Exparel (Bupivacaine) for the Treatment of Craniofacial Pain Phase 2
Active, not recruiting NCT05023460 - Treatment of Chronic Cluster Headache With TENS and ONS N/A