WHO ICTRP trial

Effect of neuromodulation device in patient suffering from migraine for…

CTRI/2024/12/078283 · Clinical Trials Registry India (CTRI) · Recruiting

Key facts

Trial ID CTRI/2024/12/078283
Public title Effect of neuromodulation device in patient suffering from migraine for prophylaxis.
Scientific title Efficacy and safety of Nerivio, a remote electrical neuromodulation device, for prophylaxis of episodic and chronic migraine: an open label, multicentric study in Indian population - NIL
Primary sponsor Dr. Reddy Laboratories Ltd
Secondary sponsors Kantar IMRB Contract Research Organization
Registry Clinical Trials Registry India (CTRI)
Recruitment status Recruiting
Study type PMS
Phase Post Marketing Surveillance
Countries India
Conditions Health Condition 1: G431- Migraine with aura Health Condition 2: G430- Migraine without aura
Interventions Intervention1: Nerivio™: Nerivio™ is an US FDA-authorized remote electrical neuromodulation (REN) device for the prophylaxis treatment of migraine with or without aura in patients 12 years old or above. The device delivers transcutaneous…
Registration date Dec 18, 2024
Target size 278
Secondary IDs DRL-NEU-003, Version 3.0 dated 25/09/2024
Registry page ctri.nic.in

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations