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Glabellar Botulinum Toxin Injections for the Treatment of Geriatric Depression (BOTDEP)

H

Helse Stavanger HF

Status and phase

Withdrawn
Phase 1

Conditions

Major Depressive Disorder
Treatment Resistant Depression
Major Depressive Episode

Treatments

Drug: Placebos
Drug: botulinum toxin A

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The effectiveness of glabellar injection of botulinum toxin type A (BTA) in treating depression has not yet been investigated in elderly patients. The study aims in addressing the question if glabellar injection of BTA is effective in treating geriatric depression.

Full description

Feedback from facial expressions is known to influence emotional experience. Treatment of muscles involved in facial expression of sadness, anger or anxiety with botulinumtoxin showed a quick, strong and sustained improvement in the symptoms of depression. As considerable proportion of patients do not sufficiently respond to existing treatment options. Especially in the elderly current treatments show limited response or are associated with side effects. Injections with BTA are considered as a very safe treatment without lasting side effects. The aim of the study is to investigate effectiveness of BTA in treating major depression in the elderly in a cross-over designed, placebo-controlled manner.

Sex

All

Ages

65 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria: Clinically relevant depressive symptoms ( defined as MADRS > 12)

Exclusion criteria: cognitive deficits that impair the participant´s ability to provide written informed consent severe depression MADRS >34 suicidality treatment with more than 3 psychotropic medications recent changes (4 weeks) in current psychotropic medication previous treatment with study drug active substance abuse bipolar disorder schizophrenia unstable medical condition usage of warfarin or NOAC bleeding disorder known hypersensitivity to study drog or any of the excipients of the formulation myasthenia gravis or Eaton Lambert syndrome presence of infection at the proposed injection sites

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Quadruple Blind

0 participants in 2 patient groups, including a placebo group

placebo
Placebo Comparator group
Description:
injections with sodium chloride
Treatment:
Drug: Placebos
botulinum toxin A
Active Comparator group
Description:
injections with botulinum toxin A
Treatment:
Drug: botulinum toxin A

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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