Autopsy report · NCT03316105
Effect of T6 Dermatome Electrical Stimulation on Gastroduodenal Motility in Healthy Volunteers
Cause of deathDrug or device supply
“Electrical device malfunction; recruitment was stopped.”
Life of this trial
- Registered 1 month after it had already started.
- Ran for about 9 months before it stopped.
- 16 participants enrolled.
- Results were posted on the registry 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Conditions
- Weight Loss
- Interventions
- Elira Investigational TENS device
- Participants
- 16
- Sites
- 1
- Countries
- United States
Trials that died the same way
- A Study for AR100DP1 in Mild to Moderate Atopic Dermatitis (AD)
“Due to the two AEs in Phase IIa study, recruiting was stopped for safety sake. The study was currently terminated.” - A Study to Assess the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Debio 4126 in Participants With Acromegaly or Functioning Gastroenteropancreatic Neuroendocrine Tumors (GEP-NETs)
“The recruitment was halted for strategic reasons” - Study of Efficacy of Association of Senna Alexandrina Mill and Associations on Functional Intestinal Constipation
“The study was interrupted by recruitment failure.” - Xenon-anesthesia on Patients Undergoing Major Liver-resection
“A device would have had to be maintained. The maintenance company is insolvent; both another maintenance company and another serviced device were not available.” - Focus on Fibre Study
“There were issues with recruitment so study was stopped”
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.