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NCT03393546

Auricular Point Acupressure to Manage Pain in Patients With Alzheimer's Disease and Related Disorders

Terminated NA Last updated 10 July 2023
What this trial tests

NA trial testing Auricular Point Acupressure in Pain in 8 participants. Terminated before completion.

Timeline
1 August 2018
Primary endpoint
8 March 2022
8 March 2022

Quick facts

Lead sponsorJohns Hopkins University
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment8
Start date1 August 2018
Primary completion8 March 2022
Estimated completion8 March 2022
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Johns Hopkins University

Who can join

Adults 21 to 85, any sex, with Pain or Alzheimer Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Pain is considered as one of the most important causal factors of behavioral and psychological symptoms in patients Alzheimer's disease and related disorders (ADRD). The investigators plan to examine the effectiveness of pain relief, pain sensory change and immune biomarkers change (measured by serum biomarkers) after the auricular point acupressure (APA). A waitlist will be used to examine the feasibility of a 4-week APA intervention. The investigators will also explore potential analgesic pathways and underpinnings of APA on pain relief.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Auricular Point Acupressure

Trials testing the same drug.

Other recruiting trials for Pain

Currently open trials in the same condition.

Other Johns Hopkins University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03393546.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing