Autopsy report · NCT01011634

Trial Comparing Intravenous and Oral Moderate Sedation for First Trimester Surgical Abortions

“7% enrollment. Study terminated after a small number of recruited patients”

The sponsor’s own words in the registry.

Life of this trial

• Registered 2 years 6 months after it had already started.
• Ran for about 1 year 6 months before it stopped.
• 18 participants enrolled.
• Results were posted on the registry 4 years 6 months after it ended.

Vital statistics

Status

Terminated

Phase

Phase 4

Sponsor

University of California, San Francisco

Sponsor type

University, hospital or other

Conditions

Undesired Intrauterine Pregnancy; First Trimester Pregnancy

Interventions

Intravenous moderate sedation versus oral medication

Participants

18

Sites

1

Countries

United States

Trials that died the same way

• Real-world Clinical Patterns Of Care And Outcomes Among AfME mRCC Patients Receiving Sunitinib as First Line Therapy.
  “The study was terminated early due to the inability to recruit the planned number of patients” (82% match in meaning)
• Alvimopan Use in Polytraumatized Patients
  “This study was terminated due to failure to enroll, a low volume of patients met criteria.” (81% match in meaning)
• GW786034 in Patients With Non Small Cell Lung Cancer 3rd Line
  “Study was terminated due to positive results seen in statistical analysis. Adequate patient enrollment was achieved.” (81% match in meaning)
• Assessment of the Effect of Tegaserod (2 mg Tid and 6 mg Tid) on Dyspeptic Symptoms in Diabetic Patients With Symptoms of Diabetic Gastropathy
  “This study was terminated early in April 2005 due to low patient enrollment” (80% match in meaning)
• Comparison of the Live Birth Rate Between the PPOS and the GnRH Antagonist Protocol in Patients Undergoing IVF
  “The study was terminated due to difficulty in recruiting patients.” (79% 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.