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Evaluating retrospective data of Nerivio Device in Chronic and Episodic Migraine

Evaluating the Effectiveness and Safety of Nerivio Device in Chronic and Episodic Migraine A Retrospective Observational Real World Evidence Analysis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/11/076750
Enrollment
300
Registered
2024-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: G437- Chronic migraine without aura

Interventions

Intervention1: Nil: Nil Control Intervention1: Nil: Nil

Sponsors

Dr Reddys Laboratories Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adults diagnosed with migraine according to the International Classification of Headache Disorders, 3rd edition (ICHD-3) criteria Patients who have been prescribed and have used REN devices within the past 12 months

Exclusion criteria

Exclusion criteria: Patients with incomplete medical records Patients with other significant chronic pain disorders Pregnant or breastfeeding women

Design outcomes

Primary

MeasureTime frame
Demographic information of the study population Categorize and assess the types of migraines duration of migraine history and patient profiles Proportion of patients showing improvement in clinical signs and symptoms of migraine after using Nerivio Reduction in migraine medication regimen Timepoint: baseline to end of 12 months

Secondary

MeasureTime frame
Incidence of Adverse Event following the use of NerivioTimepoint: Baseline to 12 months

Countries

India

Contacts

Public ContactDr Sagar Katare

Dr Reddys Laboratories limited

mayankdhore@drreddys.com8860530669

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026