Autopsy report · NCT01606618
Self-esteem and Neuro-urological Follow-up in Patients With Spina Bifida or Spinal Cord Injury
Cause of deathFunding or business
“Sponsor and investigator's decision”
Life of this trial
- Registered 2 months after it had already started.
- Ran for about 5 years 6 months before it stopped.
- 111 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Rennes University Hospital
- Sponsor type
- University, hospital or other
- Conditions
- Spina Bifida Aperta; Acquired Traumatic Spinal Cord Injury
- Participants
- 111
- Sites
- 16
- Countries
- France
Trials that died the same way
- Unipolar Microplasma Radiofrequency Device: In-vivo Histologic Study
“Per Investigator and sponsor decision” - The Effect of a Probiotic Strain on Aspirin-induced GI Damage
“Decision made by Sponsor” - Severe Acute Respiratory Syndrome Coronavirus Type 2 (SARS-CoV-2)-Related Multiple Sclerosis (MS) Vaccination Study
“Sponsor's decision” - Study to Assess the Efficacy and Safety of NTRA-2112 on Intestinal Malabsorption in Preterm Infants
“Sponsor decision”
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.