BTL-699 for the Reduction of Food Cravings

BTL

Status

Completed

Conditions

Food Cravings

Treatments

Device: Treatment with BTL-699

Study type

Interventional

Funder types

Industry

Identifiers

NCT06889298

BTL-699_CTCZ100

Details and patient eligibility

About

The goal of this clinical trial is to evaluate if the treatment with BTL-699 device is able to temporarily reduce food cravings in adults above the age of 22 years. The main question it aims to answer is:

Does the treatment with BTL-699 device provide a temporary reduction of food cravings?

Participants will be asked to:

Undergo 4 to 6 treatments
Undergo weight measurements
Complete the Food Cravings Questionnaire-Trait
Complete the Therapy Comfort Questionnaire
Complete the Satisfaction Questionnaire

Full description

This study uses a single-center, single-arm, open-label, interventional design.

Subjects reporting at least 3 to 5 weekly instances of food cravings will be enrolled. All enrolled participants will receive 4 to 6 treatments with the BTL-699 device, administered 2 to 3 days apart. The required number of treatments for each participant will be determined on a case-by-case basis by the Principal Investigator, with a minimum of four sessions.

Therapy parameters will be adjusted based on patient feedback and comfort, up to 100% of the individual's motor threshold.

Examination for possible adverse effects will be assessed at each visit.

The Food Cravings Questionnaire-Trait will be administered before the first treatment, after the last treatment, and at the two follow-up visits-2 weeks and 1 month after the final session.

The Therapy Comfort Questionnaire will be administered after the last treatment, while the Satisfaction Questionnaire will be given after the last treatment and at both follow-up visits.

The total expected duration of subject participation, from the baseline visit to study completion, is approximately three months.

Enrollment

29 patients

Sex

All

Ages

22+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

At least 3-5 self-reported episodes of food craving periods per week
Age > 22 years
Ability to determine the motor threshold of the participant. The participant's motor threshold could be established as the minimum stimulus required to induce contraction of the right thumb at least five out of 10 times
Subjects willing and able to abstain from partaking in any other weight management treatments other than the study procedure during study participation
Willingness to comply with study instructions and to return to the clinic for the required visits

Exclusion criteria

Cochlear implants
Intake disorders such as bulimia, anorexia
Borderline personality disorder
Other metal implants close to the application area (1 meter at least)
Personal history of epilepsy
Personal history of syncope
Vascular, traumatic, tumoral, infectious, or metabolic lesion of the brain, even without a history of seizure, and without anticonvulsant medication
Sleep deprivation
Alcoholism
Presence of a substance abuse or dependence (alcohol, caffeine, drugs) conditions associated with altered seizure risk
Intake of one or a combination of the following drugs forms a strong potential hazard for the application of rTMS due to their significant seizure threshold lowering potential: imipramine, amitriptyline, doxepine, nortriptyline, maprotiline, chlorpromazine, clozapine, foscarnet, ganciclovir, ritonavir, amphetamines, cocaine, (MDMA, ecstasy), phencyclidine (PCP, angel's dust), ketamine, gamma-hydroxybutyrate (GHB), alcohol, theophylline
Intake of seizure threshold lowering drugs such as: mianserin, fluoxetine, fluvoxamine, paroxetine, sertraline, citalopram, reboxetine, venlafaxine, duloxetine, bupropion, mirtazapine, fluphenazine, pimozide, haloperidol, olanzapine, quetiapine, aripiprazole, ziprasidone, risperidone, chloroquine, mefloquine, imipenem, penicillin, ampicillin, cephalosporins, metronidazole, isoniazid, levofloxacin, cyclosporin, chlorambucil, vincristine, methotrexate, cytosine arabinoside, BCNU, lithium, anticholinergics, antihistamines, sympathomimetics
Withdrawal from one of the following drugs could form a relative hazard for the application of rTMS due to the resulting significant seizure threshold lowering potential: alcohol, barbiturates, benzodiazepines, meprobamate, chloralhydrate
Systemic infection, fever
Patients with a broad range of neuropsychiatric diseases are at elevated risk for seizures. - Essentially all neurologic conditions with structural cerebral damage (e.g. stroke, multiple sclerosis, traumatic brain injury, Alzheimer's and other neurodegenerative diseases, meningoencephalitis or intracerebral abscess, parenchymal or leptomeningeal cancers) are associated with an elevated risk for seizures
Major depression (elevated seizure risk)
Hyponatremia, hypocalcemia, hypomagnesemia, hypoglycemia, hyperglycemia, renal failure/uremia, liver failure
Raised blood concentrations of pro-convulsant medications due to reduced clearance (e.g. secondary to initiation of antibiotics for treatment of infections)
Immunosuppressive therapy with cyclosporine, tacrolimus and other agents that can cause the posterior reversible leukoencephalopathy syndrome
Dialysis
Bipolar Disorder
Pregnancy or lactation, absence of medically approved contraceptive methods in females of childbearing potential
Urine drug screen positive for amphetamines, barbiturates, cannabinoids, cocaine metabolites, opiates and phencyclidine
Implanted infusion pumps
Intracardiac devices (pacemakers, heart valves, etc.)
Contradictions for the testing used in the trial, for example, the motor threshold cannot be found or quantified