Migraine meds put to the test in Real-World study
NCT ID NCT05827887
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study followed 226 adults in Israel who were prescribed ubrogepant or atogepant for their migraines. Researchers wanted to see how satisfied people were with these drugs in real-world settings, not just in a lab. Participants used an app to track their experience over 90 days, and the main goal was to measure treatment satisfaction.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
226 people
The number who actually took part.
- Started
-
Jun 2023
- Finished
-
Jan 2026
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult participants with migraine prescribed Ubrogepant or Atogepant by their physician.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Confirmed diagnosis of migraine according to the ICHD-3 upon judgement of the treating physician * The patients should be naive to the designated treatment * Ability to fill an e-diary app Exclusion Criteria: * Patients who cannot be treated with UBRO or ATO according to the applicable approved label * Patients participating in a concurrent clinical interventional study or within the last 30 days * Patients who were previously treated with rimegepant will be excluded from the study
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Migraine are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Assuta Ashdod Medical Center /ID# 260020
Ashdod, Southern District, 7747600, Israel
-
Clalit HMO /ID# 257364
Gani Tikva, 5591236, Israel
-
Edith Wolfson Medical Center /ID# 269740
Holon, Central District, 5822012, Israel
-
Hadassah Medical Center-Hebrew University /ID# 257352
Jerusalem, 91120, Israel
-
Maccabi Healthcare Services /ID# 254171
Kfar Saba, Central District, 4420123, Israel
-
Meir Medical Center /ID# 254170
Kfar Saba, Central District, 4428164, Israel
-
Shaare Zedek Medical Center /ID# 254169
Jerusalem, Jerusalem, 91031, Israel
-
Soroka University Medical Center /ID# 254551
Beersheba, Southern District, 8410101, Israel
-
Tel Aviv Sourasky Medical Center /ID# 263089
Tel Aviv, Tel Aviv, 6423906, Israel
-
The Chaim Sheba Medical Center /ID# 254550
Ramat Gan, Tel Aviv, 5265601, Israel
-
ZIV Medical Center /ID# 257360
Safed, Northern District, 13100, Israel
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Gut bacteria may hold clues to dozens of diseases
- Blood, tears and saliva: the hunt for Migraine's hidden signature
- Could your toothpaste be triggering migraines? trial puts it to the test
- Can sleep, neck pain, and fatigue explain Migraine's daily toll?
- Do Gender-Affirming hormones trigger headaches? thai survey probes the question
- Can a pill stop a migraine in two hours?