Autopsy report · NCT04435639

Using an Adjustable Compression Garment for Secondary Upper Limb Lymphoedema

“Researcher unable to continue.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 5 years 4 months before it started.
• Suspended: paused, and may or may not restart.
• 30 participants planned (an estimate, not an actual count).

Vital statistics

Status

Suspended

Phase

Na

Sponsor

Institute of Technology, Sligo

Sponsor type

University, hospital or other

Conditions

Lymphedema of Upper Arm

Interventions

Manual lymph drainage.; Coban compression bandage..; Adjustable Compression Sleeve

Participants

30 (planned, not actual)

Sites

1

Countries

Ireland

Trials that died the same way

• PICU Admission Lactate and Central Venous Oxymetry Study
  “Researcher stopped activity at institution” (74% match in meaning)
• Aspirin Resistance Following Coronary Bypass Surgery
  “The researcher had left the hospital and the project was stopped” (70% match in meaning)
• Central Hemodynamic Exercise Responses Study
  “Researcher left” (69% match in meaning)
• TubeClear® Evaluation in Pediatric Patients (Phase I)
  “Unable to recruit; study determined not feasible to continue” (65% match in meaning)
• Evaluation of Hydrocortisone, Vitamin C and Thiamine for the Treatment of Septic Shock
  “The research is no longer funded and terminated due to futility” (65% 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.