Autopsy report · NCT04345952
Calm for Cancer Patients Receiving Chemotherapy
Cause of deathRegulatory or ethics
“Study was never submitted to the IRB so never received permission to or enrolled any 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- Withdrawn before it enrolled anyone.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- Withdrawn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
- The University of Texas Health Science Center at San Antonio
- Sponsor type
- University, hospital or other
- Conditions
- Cancer Colorectal
- Interventions
- Calm Meditation Mobile App
- 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” - The Dose-Response Relationship of Rocuronium in Patients Taking Pyridostigmine
“No eligible subjects identified. Study closed with IRB.” - Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
“Study did not receive IRB approval, so did not start” - Virtual Reality and D-Cycloserine in Combat Related Psycological Trauma in Burn Service Members
“Investigator was not able to maintain IRB approval. Study never accrued subjects.”
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.