Autopsy report · NCT01637987

Nurse PIV Insertion Success With and Without Assistive Devices in Patients 0-12 Months of Age

“Combination of insufficient research staff support, insufficient subjects meeting enrollment criteria, and investigators changing role responsibilities. Administratively closed (continuing review or completion report not submitted).”

The sponsor’s own words in the registry.

Life of this trial

• Ran for about 4 years 7 months before it stopped.
• 104 participants enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

University of Nebraska

Sponsor type

University, hospital or other

Conditions

PIV Catheter Insertion; Vein Visualization

Interventions

Unassisted vein visualization; Wee Sight® Transilluminator; VeinViewer® (Christie Digital Systems, Cypress, CA)

Participants

104

Sites

1

Countries

United States

Trials that died the same way

• Assessing the Efficacy of Needling With or Without Corticosteroids in the Repigmentation of Vitiligo
  “Principal investigator made the decision to close study and not submit a renewal. Lack of fixed research personnel to carry out the study effectively.” (70% match in meaning)
• Prospective Study of Non-operative Management of SBO Without Nasogastric Tube Placement
  “Study was closed due to lack of personnel for recruitment/enrollment purposes.” (70% match in meaning)
• Triple vs High Dose Inhaled CORticosteroids
  “The study is closed due to lack of recruitment.” (68% match in meaning)
• Study to Compare the Efficacy and Safety of Micafungin Versus Conventional Amphotericin B for the Treatment of Neonatal Candidiasis
  “It was decided to discontinue the study due to insufficient recruitment.” (68% match in meaning)
• Biliary Interventions in Critically Ill Patients With Secondary Sclerosing Cholangitis (BISCIT)
  “Study was stopped due to insufficient recruitment.” (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.