Autopsy report · NCT04921982

Efficacy of Traumatic Memory Modification Using Memory Reconsolidation and Propranolol Among Adolescents With PTSD

“The study could not begin within the period of validity of the authorizations. The project has been abandoned in its initially authorized form. The final study report will not be produced.”

The sponsor’s own words in the registry.

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• Withdrawn before it enrolled anyone.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Withdrawn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

Phase 2

Sponsor

Rennes University Hospital

Sponsor type

University, hospital or other

Conditions

Post Traumatic Stress Disorder

Interventions

Propranolol; Placebo

Participants

0

Sites

10

Countries

France

Trials that died the same way

• Accuracy of Robotically Assisted Cranial Biopsies
  “The clinical study could not be commenced due to the Principal Investigator's limited availability, which has significantly impacted the feasibility of continuing the study as planned. No safety concerns or adverse events were detected.” (70% match in meaning)
• Technology Knowledge Optimization in Type 1 Diabetes (TeKnO T1D): Parents
  “Investigator left the institution and is relinquishing the award supporting this study. The study will not launch.” (69% match in meaning)
• Study of Pemetrexed for Second-Line Pancreas Cancer
  “At interim analysis the study did not meet the response criteria to continue” (69% match in meaning)
• Anti-NY ESO-1 mTCR Peripheral Blood Lymphocytes
  “Due to lack of accrual the study was formally terminated on 01-JUL-2020. Primary Completion and Study Completion Dates have been revised based accordingly based on respective definitions” (68% match in meaning)
• Human IL-15 (rhIL-15) and Obinutuzumab for Relapsed and Refractory Chronic Lymphocyte Leukemia
  “The study was closed after \> 1 year of inactivity.” (68% match in meaning)

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.