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Efficacy of Postural Restriction in Treating Benign Paroxysmal Positional Vertigo

P

Prince of Songkla University

Status

Unknown

Conditions

Benign Paroxysmal Positional Vertigo

Treatments

Behavioral: Postural restriction
Behavioral: Normal daily activity

Study type

Interventional

Funder types

Other

Identifiers

NCT02475239
REC 57-0082-13-1

Details and patient eligibility

About

The standard treatment of posterior semicircular canal benign paroxysmal positional vertigo is the canalith repositioning procedure or the Epley maneuver. Based on the present literature, there is controversy on the efficacy of post-maneuver postural restrictions.The aim of this study was to conduct a randomized controlled trial to compare the treatment efficacy of post-maneuver postural restriction with CRP alone in patients with posterior semicircular canal benign paroxysmal positional vertigo.

Full description

Benign paroxysmal positional vertigo is the most common cause of vertigo. Based on the present literature, there is controversy on the efficacy of post-maneuver postural restrictions.Some study designs were not randomized controlled trials. The present study offers an alternative way of postural restriction to maintain postural restriction as much as possible.

Enrollment

186 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with unilateral posterior semicircular canal benign paroxysmal positional vertigo and
  • A negative neurologic examination

Exclusion criteria

  • Secondary benign paroxysmal positional vertigo caused by trauma head injury, inner ear surgery, viral labyrinthitis or Meniere's disease
  • Patients with central vertigo, cervical spine, neurologic, otologic, psychiatric diseases
  • Patients who used medications that affected the neurologic and otologic systems for less than 48 hours

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

186 participants in 2 patient groups

Postural restriction
Experimental group
Description:
The patients were instructed to avoid head movements, wear a soft collar during the daytime, wear a supporting pillow and sleep in the semi-upright position at a 45 degree head elevation from the horizontal plane during the nighttime for 48 hours.
Treatment:
Behavioral: Postural restriction
Normal daily activity
Active Comparator group
Description:
The patients did not follow any postural restrictions and were asked to live as normally as possible.
Treatment:
Behavioral: Normal daily activity

Trial contacts and locations

1

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Central trial contact

Yuvatiya Plodpai, MD

Data sourced from clinicaltrials.gov

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