Autopsy report · NCT05596058
Non-pharmacological Treatments in Migraine.
Cause of deathSlow enrollment
“Due to the unavailability of the subjects who gave the consent to participate to the study protocol”
Life of this trial
- Ran for about 1 year 5 months before it stopped.
- 30 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- University of Trieste
- Sponsor type
- University, hospital or other
- Conditions
- Migraine
- Interventions
- dual task protocol: active exercises with concomitant cognitive training in executive functions; active exercise; cognitive task only
- Participants
- 30
- Sites
- 1
- Countries
- Italy
Trials that died the same way
- Use of Goggle Balloon to Improve Cecal Intubation During Colonoscopy
“no subjects consented due to competing studies” - Escitalopram in Anxiety Associated Chronic Obstructive Pulmonary Disease (COPD) Exacerbations
“Study was not given ethical approval- a alternative protocol required” - Identification of Elderly Patients in Need of Palliative Care by Family Physicians
“We were not able to recruit participants to enrol the study. As it was not able, the investigation team decided not to proced.” - Evaluation of Safety and Efficacy of the EndoLift Liver Retractor
“The study was terminated. Six subjects were consented \& all were withdrawn before any study activities took place.” - FASTMAS (Fast-Fail Trials in Mood and Anxiety Spectrum Disorders) Kappa Opioid Receptor Phase 1 Study
“Funding for the study ended with one subject consented, but not randomized”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.