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Targeting fear memory by disrupting the process of reconsolidation: A new intervention for panic disorder.

Targeting fear memory by disrupting the process of reconsolidation: A new intervention for panic disorder. - Reconsolidation Intervention for Panic Disorder.

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON47318
Enrollment
60
Registered
2016-06-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-23

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

Conditions

Anxiety Disorder. Panic Disorder

Interventions

One of the following: 1. 35% CO2-enriched air inhalation followed by the administration of 40 mg propranolol. 2. A placebo-inhalation followed by the administration of 40 mg propranolol. 3. 35

Sponsors

Universiteit van Amsterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: A primary diagnosis of panic disorder according to DSM-V.

Exclusion criteria

Exclusion criteria: * other relevant treatment for panic disorder at the time of study - e.g., CBT * diagnosis of psychosis * use of psychotropic medication * A current state of asthma or COPD, which necessitates medication use * history of respiratory diseases (asthma or COPD in the past does not lead to exclusion) * history of cardiovascular diseases or irregular heartbeat * history of cerebrovascular diseases * history of severe allergic reactions to propranolol, which necessitated hospitalisation * cerebral aneurysm among first-degree relatives * Heart rate 180/100 * epilepsy * any medication contra-indicative of the use of propranolol * pregnancy

Design outcomes

Primary

MeasureTime frame
Individual scores on the Panic Disorder Severity Scale. Presence of panic disorder according to DSM V criteria

Secondary

MeasureTime frame
Individual scores on the Panic Appraisal Inventory, Mobility Inventory, Body Sensations Questionnaire, and Agoraphobic Cognitions Questionnaire will be used as secondary study parameters. In addition, willingness to inhale 35% CO2 is used as a secondary study parameter.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)