Autopsy report · NCT01144741

Survey Study and Records Review of Treatment Outcomes in Freeman-Sheldon Syndrome

“Insufficient patient enrolment”

The sponsor’s own words in the registry.

Life of this trial

• Registered 4 months after it had already started.
• Ran for about 12 years 4 months before it stopped.
• 2 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Sponsor

Freeman-Sheldon Research Group, Inc.

Sponsor type

University, hospital or other

Conditions

Freeman-Sheldon Syndrome; Arthrogryposis Distal Type 2A; Whistling Face Syndrome; Craniocarpotarsal Dysplasia; Craniocarpotarsal Dystrophy; Freeman-Sheldon Syndrome Variant

Interventions

PTSD Checklist-Civilian (PCL-C); Modified Flanagan Quality of Life Scale; Center for Epidemiologic Studies Depression Scale (CES-D); Functional Enquiry (or Review of Systems) Form; Study of Therapeutic Outcomes and Practices in Freeman-Sheldon Syndrome (STOP-FSS) Questionnaire; FSRG Semi-Structured Quality of Life Interview (FSRG SSQLI)

Participants

2

Sites

1

Countries

United States

Trials that died the same way

• Enzyme Replacement Therapy in Fabry Disease
  “Difficulties in the patient's enrolment” (86% match in meaning)
• The Effect of Probiotics on Response to Therapy and on Adverse Effect in Patients Treated With Colchicine for Familial Mediterranean Fever.
  “no patient enroled” (84% match in meaning)
• Human Brain Adaptation to Chronic Pain and Its Effects on Opioid Use
  “Insufficient patient enrollment.” (79% match in meaning)
• Phase 3 Trial for AML Patients in CR2 Comparing 8Gy TBI /Fludarabine to Conditioning With TBI 12Gy/Cyclophosphamide
  “insufficient patient recruitement” (78% match in meaning)
• The CEASE Study: Computer Based Educational Module for the Reduction of Arthralgia Syndrome Associated With Endocrine Therapy for Breast Cancer
  “Unable to recruit sufficient patients” (76% 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.