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The Efficacy of Bioresonance Therapy for smoking Cessation.

The Efficacy of Bicom2000 Bioresonance Device for smoking Cessation

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180322001
Enrollment
342
Registered
2018-03-22
Start date
2018-03-24
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking cessation Bioresonance therapy smoking cessation bicom2000

Interventions

each subject will have one session of a standardized intervention lasting for about 45 minutes using the BICOM2000 device as per the manufactured company protocol that is adopted by Waqf Albarakah Ant
Smoking Charity Clinic. The assessors will be healthcare workers who will get a professional training on the use of bioresonance device in Waqf Albarakah Anti&#45
Smoking Clinic. Prior to the intervention&#44
subjects will be asked to consume one cigarette and fill the cigarette ash and its non&#45
smoked remnants into two glass tubes. Then after&#44
the glass tubes containing cigarette remnants and ash will be distinctly positioned into the bioresonance device has input electrodes Active bioresonance therapy will be applied via a pre&#45
set program combination that deliver the electromagnetic waves to the subject over 4 stages.The amplification for the simulated bioresonance therapy (placebo arm) will be set to zero and the input and
so that no oscillation could go in or out the device. The participants will be unable to know which of the treatment variants they will be exposed to since both intervention program combinations will
smoked remnants into t
Experimental Device,Placebo Comparator Device

Sponsors

Investigator
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: subjects for this study will be male cigarette smokers who decide to quit smoking. The study will be restricted to male patients since both centers in which the study will be conducted are designed to serve male patients only. Subjects have to be between 18 and 75 years of age.

Exclusion criteria

Exclusion criteria: Patients who are suffering from heart diseases and/or psychiatric disorders interfering with their insights or judgments, such as schizophrenia or major depression will be excluded. Additionally, Patients who have prior exposure to pharmacological modalities for smoking cessation in the last 3 months will be considered illegible to avoid possible therapeutic contamination.

Design outcomes

Primary

MeasureTime frame
Biochemically confirmed prolonged abstinence rate from smoking 6 Months after the intervention CO level in exhaled air

Secondary

MeasureTime frame
7-day and 1 month point prevalence abstinence rate from smoking 1 week , 1 month self report

Countries

Saudi Arabia

Contacts

Public ContactHani Almalki

Saudi Board of Community Medicine, department of Community Medicine , College of Medicine , Taibah U

hanialmalki@yahoo.com00966542631632

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026