Study protocol Improving inpatient GHB detoxification with baclofen: a proof of concept and dose-finding study

BackgroundGamma-hydroxybutyric acid (GHB) use disorder (GUD) is well known for its severe withdrawal syndrome. Currently, tapering with pharmaceutical GHB is the preferred option to mitigate withdrawal. The gamma-aminobutyric acid (GABA)-B receptor agonist baclofen could improve GHB detoxification, due to its longer half-life than pharmaceutical GHB and specific GABA-B receptor activation. However, clinical data on baclofens effectiveness to manage GHB withdrawal is limited. We aim to explore potential benefits of baclofen as an add-on to pharmaceutical GHB tapering in patients with GUD. MethodsThis prospective, non-randomized, clinical trial consists of two phases: 1) a proof-of-concept phase (n=10) and 2) a dose-finding phase (n= 18). Primary objective of the proof-of-concept phase is to assess whether baclofen add-on therapy reduces the need for pharmaceutical GHB during inpatient detoxification. Safety and feasibility will also be assessed. Aim of the dose-finding phase is to explore the optimal baclofen dosage when used as add-on therapy during inpatient GHB detoxification. Criteria to start the second phase are that baclofen add-on therapy leads to a dose reduction of pharmaceutical GHB without severe side effects. GHB withdrawal symptoms and baclofen side effects will be monitored during GHB detoxification, using questionnaires. DiscussionWe expect that baclofen add-on therapy will reduce the need for pharmaceutical GHB during inpatient GHB detoxification. This will likely result in a less intensive detoxification process for patients and will improve the overall feasibility of GHB detoxification. If the outcome of the current phase II trial is positive, either a replication phase II trial with a randomized blinded design or a lager phase III trial, would be a logical follow-up study to confirm the safety, feasibility and efficacy of baclofen add-on therapy during inpatient GHB detoxification. Trial registrationThis study protocol is approved by the Medical Ethical Research Committee Oost-Nederland and Central Committee on Research Involving Human Subjects. The study is registered in the Clinical Trial Information System under EU CT-number: 2023-506167-34-02.