Autopsy report · NCT03500406
Penile Lengthening Pre-Penile Prosthesis Implantation
Cause of deathStaffing, sites or logistics
“PI changed subspecialties and no longer had access to main study population”
Life of this trial
- Ran for about 1 year before it stopped.
- 24 participants enrolled.
- Results were posted on the registry 9 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Mayo Clinic
- Sponsor type
- University, hospital or other
- Conditions
- Erectile Dysfunction
- Interventions
- RestoreX; Control
- Participants
- 24
- Sites
- 2
- Countries
- United States
Trials that died the same way
- Levonorgestrel-Intrauterine System (LNG-IUS) Insertion in the Postpartum Period
“No recruitment occurred and the PI stopped the study” - Yttrium-90 (TARE-Y90) in Children, Adolescents, and Young Adults With Liver Tumors
“PI left organization and discontinued study” - Affective Processing in Depression and Epilepsy
“PI wanted to discontinue study.” - Isometric Intervention for Lateral Elbow Tendinopathy
“PI no longer at the institution; departmental permission to deactivate study” - Noninvasive Cardiac Output Measurements in Patients With Pulmonary Hypertension Undergoing Right Heart Catheterization With Acute Vasodilator Testing
“The PI closed this study and went to another institution.”
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.