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Muscarinic modulation of human electroencephalography (EEG) activity using scopolamine

Measuring the effects of intravenous scopolamine on the human EEG in healthy volunteers

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12622000228785
Acronym
HIGGS
Enrollment
12
Registered
2022-02-09
Start date
2021-06-14
Completion date
2021-12-10
Last updated
2026-01-05

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

Conditions

None listed

Brief summary

Depression is one of the leading health burdens in New Zealand. Currently prescribed medicines are ineffective in approximately one third of patients and so new treatments are needed. Some clinical trials indicate that the anti-nausea drug scopolamine may have anti-depressant effects. In this study we are investigating the pharmacokinetics and pharmacodynamic effects of scopolamine in healthy volunteers at doses similar to that being used in studies of depression to understand the effects of scopolamine on brain function

Interventions

Sponsors

The University of Auckland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

• Male or female, aged 18 years or above and less than 60. • In the Investigators’ opinion, is able and willing to comply with all trial requirements. • Participant is willing and able to give informed consent for participation in the trial.

Exclusion criteria

• Female participant who is pregnant, lactating or planning pregnancy during the course of the trial. • Regular use of any medication deemed to be contraindicating as judged by the attending study clinicians. • Contraindication to the use of scopolamine or glycopyrrolate according to manufacturer guideline • Significant renal or hepatic impairment. • Participants with glaucoma • Cardiovascular conditions including abnormal heart rate and blood pressure checked at screening. • History of psychiatric illness. • Any unstable medical or neurologic condition. • Problematic substance dependence in previous 3 months • Inability to speak or read English. • Any other condition judged by the treating clinician as likely to impact on the ability of the participant to complete the trial.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026