Different Treatments With the TRV Reposition Chair

NCT ID: NCT03541018

Last Updated: 2022-07-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-01-01

Study Completion Date

2022-01-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To investigate which treatment option (reposition maneuver) with the TRV chair that is the most effective in patients diagnosed with benign paroxysmal positional vertigo (BPPV). Subtypes of BPPV will be examined after randomization to specific treatments.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Patients diagnosed with BPPV with subtypes of either posterior canalolithiasis or lateral cupulolithiasis will we considered for enrollment. Each subgroup of patients will undergo randomization for a specific treatment.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Benign Paroxysmal Positional Vertigo

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Posterior canalolithiasis

Type of repositional maneuvre

Group Type EXPERIMENTAL

Type of repositional maneuvre

Intervention Type PROCEDURE

Patients randomized to 2 different repositional maneuvres related to the subtypes of BPPV

Lateral cupulolithiasis

Type of repositional maneuvre

Group Type EXPERIMENTAL

Type of repositional maneuvre

Intervention Type PROCEDURE

Patients randomized to 2 different repositional maneuvres related to the subtypes of BPPV

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Type of repositional maneuvre

Patients randomized to 2 different repositional maneuvres related to the subtypes of BPPV

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Age above 18 years of age
* Medical history compatible with BPPV
* Verification of BPPV with either Dix-Hallpike Maneuver or Supine Roll Test.

Exclusion Criteria

* Former treatment with a repositional Chair
* Not being able to participate or cooperate in the treatment provided by the TRV Repositional Chair
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Aalborg University Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Dan Dupont Hougaard

MD, Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Dan D Hougaard, MD

Role: PRINCIPAL_INVESTIGATOR

Aalborg University Hospital, Denmark

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of Otolaryngology, Head & Neck Surgery and Audiology

Aalborg, North Denmark, Denmark

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Denmark

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

VEST01

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.