Autopsy report · NCT00855153
Virtual Reality and D-Cycloserine in Combat Related Psycological Trauma in Burn Service Members
Cause of deathSlow enrollment, also regulatory or ethics
“Investigator was not able to maintain IRB approval. Study never accrued subjects.”
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- Withdrawn before it enrolled anyone.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- Withdrawn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
- United States Army Institute of Surgical Research
- Sponsor type
- US federal agency
- Conditions
- Psychological Trauma
- Interventions
- VR (Virtual reality); D-Cycloserine
- 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” - Calm for Cancer Patients Receiving Chemotherapy
“Study was never submitted to the IRB so never received permission to or enrolled any subjects” - Supervisory Neglect, Non-Accidental Trauma, Brief Intervention, and Treatment Referral
“Study was never initiated. No IRB approval obtained, and no participants enrolled.” - 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.