Trigeminal Neuralgia Clinical Trial
Official title:
Efficacy and Complications of Microvascular Decompression - a Prospective Systematic Study of 115 Trigeminal Neuralgia Patients
NCT number | NCT04445766 |
Other study ID # | H-16019808 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | May 1, 2012 |
Est. completion date | October 31, 2020 |
Verified date | March 2022 |
Source | Danish Headache Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The study is a non-interventional prospective observational study in patients with trigeminal neuralgia that undergoes micovascular decompression. The aim is to evaluate the efficacy and complications 2 years after microvascular decompression
Status | Completed |
Enrollment | 115 |
Est. completion date | October 31, 2020 |
Est. primary completion date | October 31, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age 18 years or older. - Most give Signed informed Consent. - Must fullfil the ICHD-3 beta diagnostic criteria for classical TN.Patients with purely paroxysmal TN and patients with TN with concomitant persistent facial pain will be included. - If the ICHD-3 beta diagnostic criteria is fulfilled and if complete clinical history, neurological and physical examination and a 3.0 Tesla MRI do not raise any suspicion of another causative disease such as painful posttraumatic trigeminal neuropathy or symptomatic TN, subjects with sensory abnormalities detected at clinical neurological examination are also included. - Has had a 3.0 Tesla MRI according to the trigeminal neuralgia protocol, prior to the surgical intervention. - Semi-structured interview and neurological examination by the independent assessors prior to neurosurgical intervention. - Has tried at least one, preferably two, sodium channel blocker (either carbamazepine or oxcarbazepine) before referral to neurosurgery. Exclusion Criteria: Subjects will be excluded if one of the following exclusion criteria is met: - Psychiatric or mental illness or condition that might interfere with the ability of the patients to fill in the Informed Consent and questionnaires. - Previous microvascular decompression as a treatment for trigeminal neuralgia |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Danish Headache Center |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Degree of pain relief 2 years after MVD | Barrow Neurological Institute pain intensity score (BNI) | 2 years | |
Primary | Degree of complication rate 2 years after MVD | The frequency of predefined major and minor complications | 2 years |
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