This is an observational study conducted to observe how subjects with dizziness and dizziness associated symptoms are managed in primary care setting in India.
- Conditions
- Health Condition 1: G89-G99- Other disorders of the nervous system
- Registration Number
- CTRI/2018/11/016408
- Lead Sponsor
- Abbott Healthcare Private Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 1000
1.Adult male and female patients (aged >=18 years) presenting with dizziness in primary care
2.Patients willing to participate in the registry and provide informed consent for participation
3.Patients who are willing and competent to sign and date a patient authorization form (PAF) for participation in the study
1.Pregnant and lactating women
2.Patients with dizziness requiring hospitalization for any cause
3.Any condition that in the opinion of the investigator does not justify the patientâ??s inclusion in the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine clinicoepidemiological profile of patients presenting with dizziness in the primary care setting <br/ ><br>Timepoint: 1. Base to Week 1 <br/ ><br>2. Baseline to Week4
- Secondary Outcome Measures
Name Time Method Management practices <br/ ><br>a. Number and percentage of patients advised to undergo routine assessments/advanced <br/ ><br>assessments <br/ ><br>b. Number and percentage of patients being advised lifestyle modification (change in <br/ ><br>smoking habit/alcohol consumption/diet/exercise/both), and/or pharmacotherapy (betahistine, <br/ ><br>prochlorperazine and cinnarizine monotherapy, and cinnarizine fixed dose combination <br/ ><br>therapy) and/or referred to specialists for further managementTimepoint: Number and percentage of patients advised for advanced assessment or lifestyle modification -From 1. Baseline to week1 , 2. Week1 and week4. <br/ ><br>