| Registry | NCT03010761 |
|---|---|
| Status | Terminated - all participants finished the trial |
| Phase | Phase 2 |
| Study type | Interventional; randomized, parallel, masking: quadruple, treatment |
| Enrollment | 90 (Actual) |
| Sponsor | China Medical University Hospital (Other) |
| Conditions | Addiction |
| Interventions | escitalopram, Moclobemide, Placebo - Cap (Drug) |
| Dates | start 2016-01-14, primary completion 2018-01-31, completion 2018-01-31, first posted 2017-01-05, last updated 2019-07-24 |
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No medication existed for BQ dependence. No clinical trials existed for the drug therapy. Previous study showed that BQ possessed the antidepressant effect via pathway of monoamine oxidase A (MAO-A). An animal model also found that the arecoline from BQ has a property as MAO-A inhibitor. Therefore, the investigators hypothesized that inhibition of the MAO-A or antidepressants might reduce the BQ addiction severity.
The investigators will conduct the randomization and double blinded with placebo controlled study with 90 participants with BQ dependence from the Family Medicine and ear, nose, and throat (ENT) outpatient department (OPD). All participants shall agree the informed consent. The range of age is from 18 to 65 years old. The participants are diagnosed as BQ use disorder without other psychiatry co-morbidity, according to the Diagnostic and Statistical Manual (DSM)-V criteria. Those who have severe physical illness, psychiatric illness, and other substance use disorder except cigarettes are excluded. All participants receive the semi-structure interview by DSM-V, International Classification of Diseases (ICD)-10, and Mini International Neuropsychiatric Interview by the psychiatrist. Before the intervention, the participants will finish their basic data, daily amount of cigarettes, betel nut, medical history and psycho-social rating scales. Next, in addition to counseling, the investigators will continue or modify the optimal antidepressants based on the previous results.
The investigators will evaluate their BQ use condition as what has been measured in the natural observation study of the first year. The investigators will check the outcome measurement by visual analog scale, betel quid withdrawal severity scale, Yale-Brown Obsessive-Compulsive (Y-BOCS) - betel quid (BQ) scale. The investigators also followed their hamilton depression scale; Beck depression index; and Beck anxiety index in the baseline, 2nd, 4th, 6th , and 8th week. The investigators also obtained the participants' gene type if the participants also agree for the prediction of oral cancers.
We'll conduct the betel-quid (BQ) dependence clinical trial since 2016. Eligible cases will be enrolled for the following 8 week double-blinded placebo controlled trial. The groups will be divided into three groups. Outcome measures include BQ use condition, addiction severity rating scale, emotional rating scale including Beck Anxiety Index (BAI), Beck Depression Index (BDI), Hamilton Depression Scales (HAMDs), and urine BQ metabolites.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| medication pills 1: escitalopram 10mg | Experimental | Drug: escitalopram | 10mg once daily, 8 weeks |
| medication pills 2: moclobemide 150mg | Experimental | Drug: Moclobemide | 150mg once daily, 8 weeks |
| medication pills 3: Placebo - Cap | Experimental | Drug: Placebo - Cap | placebo once daily, 8 weeks |
Sex: Male, ages: 14 Years to 70 Years, accepts healthy volunteers
Inclusion Criteria: * DSM-V criteria suitable for betelnut use disorder * No severe physical disorder * No major psychiatric illness * Chinese Speaker Exclusion Criteria: * Severe physical disorder * Major psychiatric illness * Inability to understand the whole protocol