Autopsy report · NCT02672371
The Effects of Sensory Training On Pain Modulation, Cognition and Time to Fatigue in Healthy Adults
Cause of deathFunding or business, also regulatory or ethics
“Study was not approved for the IRB; we then had no funds to reapply”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Na
- Sponsor
- Spaulding Rehabilitation Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Healthy Participants
- Interventions
- Active eMNS; Sham eMNS
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
“Study never approved by the IRB. Was not initiated” - Suprainguinal Fascia Iliaca Compartment Block in Direct Anterior Approach to Total Hip Arthroplasty
“Study never approved by IRB or initiated” - Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
“Study did not receive IRB approval, so did not start” - Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval” - Real-time 3-Dimensional Echocardiography for Assessment of Cardiac Function and Congenital Heart Disease
“Study did not receive IRB approval.”
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.