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Clinical Trial Summary

This study aims to investigate efficacy of two different intravenous drugs (dimenhydrinate and piracetam) in the symptomatic management of peripheral vertigo.

The patients will be randomized in two groups according to symptomatic treatment modalities: Dimenhydrinate (100 mg) and piracetam (2 g) will be given in 100 cc normal saline in 30 minutes. Each patient will be asked if her/his vertigo symptoms resolved or not, according to a numeric rating scale (0=no vertigo, 10=worst possible vertigo). The patient will be rate the intensity of symptoms in the following times:

- Numeric rating scale (1 to 10): Admission

- Numeric rating scale (1 to 10): After the study drug (No ambulation)*

- Numeric rating scale (1 to 10): After the study drug (Ambulation)*

- Ambulation refers to head movements or walking in the room, if applicable.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01890538
Study type Interventional
Source Kocaeli University
Contact
Status Completed
Phase Phase 4
Start date June 2013
Completion date May 2014

See also
  Status Clinical Trial Phase
Recruiting NCT05676216 - Sodium Bicarbonate for Acute Peripheral Vertigo N/A
Recruiting NCT05586763 - Comparison of Efficacy of Metoclopramide , Promethazine and Prochloroperazine in the Treatment of Vertigo. Phase 3