Kava for the Treatment of Generalised Anxiety Disorder: A Double-Blind Randomised Placebo-Controlled Trial (KGAD)

University of Melbourne

Status and phase: Completed; Phase 4

Conditions: Generalized Anxiety Disorder

Treatments: Dietary Supplement: Placebo; Dietary Supplement: Kava (240mg of kavalactones per day)

Study type: Interventional

Funder types: Other

Identifiers

NCT02219880

137/14

Details and patient eligibility

About

The use of Kava in Generalised Anxiety Disorder: an 18-week double-blind, randomised, placebo-controlled study.

Full description

The primary aim is to confirm the efficacy and safety of Kava compared to placebo in Generalized Anxiety Disorder (GAD). Secondary aims of the study are to confirm the relationship between specific genetic variations and response to Kava, and to explore the effects of Kava on the expression of specific genes.

Consenting participants will be randomly allocated to take either Kava or placebo over 18 weeks. They will be assessed at regular interviews throughout the trial and will have four blood tests (liver function tests to monitor participant safety, and collection of genetic material providing information on neurochemistry). The design of the study is a multi-centre, 18-week, 2-arm, double-blind randomised clinical trial (RCT) using a standardised pharmaceutical-grade water-soluble extract of Kava (240mg of kavalactones per day) versus placebo in 210 adults with GAD.

Enrollment: 178 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

To be considered for inclusion in this study, participants will be required to meet the following criteria:

• Aged between 18-70 years
• Meets the Diagnostic and Statistical Manual (DSM) IV and DSM-V diagnostic criteria for generalised anxiety disorder (GAD) based on structured interview (Mini International Neuropsychiatric Interview-Plus 6 [MINI-Plus 6]. Note that while the MINI-Plus 6 uses the DSM-IV criteria, the same criteria are used in the DSM-V).
• Presents with anxiety (Hamilton Anxiety Rating Scale ≥ 18) at the time of study entry
• Fluent in written and spoken English
• Provides a signed copy of the consent form

Participants are ineligible to enter the trial if they have any of the following conditions:

• Primary diagnosis other than GAD
• Presentation of moderate to severe depressive symptoms (Montgomery-Asberg Rating Scale: MADRS ≥ 18 at time of study entry or ≥ 24 at any time during study)
• Presentation of suicidal ideation (≥ 3 on MADRS suicidal thoughts domain at time of study entry or at any time during study)
• Current diagnosis of bipolar disorder or schizophrenia on structured interview (MINI Plus)
• Current substance/alcohol use disorder on structured interview (MINI Plus) Page 21 of 39 Commercial-in-Confidence
• Currently taking an antidepressant, mood stabiliser, antipsychotic, anticonvulsant, warfarin or thyroxin, or current regular use (more than 2 days per week) of a benzodiazepine or opioid-based analgesic
• Current use of a psychotropic nutraceutical (e.g. St John's wort)
• Previous intolerance to kava
• Three or more failed trials of pharmacotherapy for the current GAD episode
• Recently commenced psychotherapy (within four weeks of study entry)
• Known or suspected clinically unstable systemic medical disorder
• Diagnosed hepato-biliary disease/inflammation
• Elevated liver enzymes at baseline blood test
• Pregnancy or breastfeeding, or trying to conceive
• Not using medically approved contraception (including abstinence) if female and of childbearing age
• Unable to participate in all scheduled visits, treatment plan, or other trial procedures according to the protocol (except for the optional genetic component)

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

---

178 participants in 2 patient groups, including a placebo group

Placebo

Placebo Comparator group

Description:

Inert tablets matched for colour, size and consistency to active arm treatment. Both treatment arm tablets will match in appearance, and neither participants nor the trial clinicians will know what they are taking.

Treatment:

Dietary Supplement: Placebo

Kava - standardised 240mg kavalactones

Experimental group

Description:

Standardised 240mg kavalactones per day - fixed dose regime of two tablets of kava twice per day

Treatment:

Dietary Supplement: Kava (240mg of kavalactones per day)