Nasal Carbon Dioxide for the Symptomatic Treatment of Classical Trigeminal Neuralgia

NCT ID: NCT02473016

Last Updated: 2017-11-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-09-30
• Study Completion Date: 2017-04-30

Brief Summary

A placebo-controlled, single-blind study to evaluate the safety and preliminary efficacy of nasal carbon dioxide for the symptomatic treatment of classical trigeminal neuralgia.

Conditions

Trigeminal Neuralgia

Keywords

Classical Trigeminal Neuralgia

Study Design

• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Treatment

All subjects will receive both Active (Carbon Dioxide Drug Delivery System) and Placebo. This is a single-blind study so subjects will not know the order. Subjects will receive 3 doses of active and 3 doses of placebo. One dose is a 60 second delivery of CO2 or placebo. At the discretion of the investigator, subjects may receive up to 3 additional doses of CO2.

Group Type: EXPERIMENTAL

Carbon Dioxide Drug Delivery System (CDDS)

Intervention Type: DRUG

Doses will be administered to the nostril on the side of the trigeminal episode \[ipsilateral nostril\].

Interventions

Carbon Dioxide Drug Delivery System (CDDS)

Doses will be administered to the nostril on the side of the trigeminal episode \[ipsilateral nostril\].

Intervention Type: DRUG

Other Intervention Names

Nasal CO2; Nasal Carbon Dioxide

Eligibility Criteria

Inclusion Criteria

• Male and female, 18 years of age and older.
• History of classical trigeminal neuralgia with or without persistent background facial pain, not secondary, as defined by International Classification of Headache Disorders (ICHD), third edition, beta version (ICHD-3 beta, Cephalalgia 2013).
• Diagnosis of trigeminal neuralgia (TN) for at least 60 days prior to enrollment.
• Experience pain with a score of at least 5 on a 0-10 scale during a typical TN episode as reported by subject. Note: Prior to treatment pain score must a 5 or greater on a VAS.
• History of unilateral typical TN pain predominantly in the V2 branch of the trigeminal nerve.
• Absence of a significant structural lesion (e.g., a tumor) as the cause of pain as shown in at least one neuro-imaging study.
• On stable dose of all medications, including those for the treatment of TN prevention/prophylaxis, for at least 14 days prior to baseline (including, but not limited to, verapamil, lithium, melatonin, any anticonvulsant, any systemic corticosteroid or steroid injection, occipital nerve block, other cranial or extracranial nerve block, or any neurostimulation treatment). Note: Subjects are allowed to use their usual standard of care for the acute/abortive treatment of trigeminal neuralgia attacks 60 or more minutes after the initial dose, provided it is approved by the investigator.
• Capable of completing a diary.
• Able to provide written Informed Consent.

Exclusion Criteria

• Are unable to comply with protocol requirements.
• Have recent of alcohol or drug abuse within 2 years prior to study enrollment.
• Current major psychiatric disorder: suicidal ideation, bipolar, panic disorder, schizophrenic, or psychosis. Subjects who are documented as clinically stable and not exhibiting symptoms related to their psychiatric disorder are eligible.
• History of asthma (other than mild or intermittent).
• Have an existing serious unstable systemic disease (e.g., severe emphysema, other respiratory diseases, heart disease, etc.) that precludes participation.
• Clinically significant nasal disorder (deviated septum, presence of polyps, evidence of significant congestion, rhinitis, or other nasal abnormalities) that prevents unrestricted breathing through each nostril.
• Currently on anticoagulants or have a diagnosis of a bleeding disorder.
• Current diagnosis of fibromyalgia, temporomandibular disorders (TMD), odontogenic pain or other orofacial pain.
• Surgery for treatment of TN within 30 days prior to screening. Note: Investigator must ensure that patients who have had surgery have recovered and are not experiencing any side effects from surgery for treatment of TN
• Females who are pregnant or breast-feeding and/or plan to become pregnant or to breast-feed during study participation or within 30 days after treatment.
• Participation in a previous study with nasal CO2.
• Participation in another investigational drug study within 30 days prior to randomization.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Capnia, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

University of California, Los Angeles (UCLA)

Los Angeles, California, United States

Meridien Research

Tampa, Florida, United States

Columbia University Medical Center

New York, New York, United States

University of Pittsbugh Medical Center (UPMC)

Pittsburgh, Pennsylvania, United States

Medical University of South Carolina (MUSC)

Charleston, South Carolina, United States

University of Virginia

Charlottesville, Virginia, United States

Countries

United States

Other Identifiers

C402

Identifier Type: -

Identifier Source: org_study_id