Autopsy report · NCT01524185

FamilyLive Feasibility and Effectiveness Study

“There were not enough eligible families and trained clinicians to conduct RCT.”

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• Withdrawn before it enrolled anyone.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Withdrawn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

Early Phase 1

Sponsor

Hugo W. Moser Research Institute at Kennedy Krieger, Inc.

Sponsor type

University, hospital or other

Conditions

Mood Lability; PTSD; Anxiety

Interventions

FamilyLive; Standard Mental Health Treatment

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Evaluation of Yoga for the Treatment of Pediatric Headaches
  “Enrollment proceeded too slowly to conduct study as RCT.” (69% match in meaning)
• Craniofacial Applications of 3D Printing
  “There was lack of internal staff support and could not enroll participants.” (64% match in meaning)
• A Single-center Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of LCAR-L10D Cell Formulations Targeting CD19 and CD22 in Patients With CD19- and/or CD22-Positive Relapsed/Refractory B-cell Lymphoma
  “Suitable patients were not recruited” (63% match in meaning)
• Midfoot Fusion Bolt (MFB) in the Early Stage of Diabetic-neuropathic Charcot Feet
  “The study was stopped because there were not enough eligible patients to complete the study.” (62% match in meaning)
• African American Families Fighting Parental Cancer Together
  “Insufficient patients meet eligibility requirements.” (62% 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.