Autopsy report · NCT01391715
Double-dose Rabeprazole Accelerates and Sustains the Control of Symptoms in Patients With NERD
Cause of deathSlow enrollment
“patients could not be recuited within study duration”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Phase 3
- Sponsor
- Inje University
- Sponsor type
- University, hospital or other
- Conditions
- Gastroesophageal Reflux Disease
- Interventions
- rabeprazole; standard dose rabeprazole
- Participants
- 0
- Sites
- 1
- Countries
- South Korea
Trials that died the same way
- Use of Hand Prosthesis With Direct Nerve Stimulation for Treatment of Phantom Limb Pain
“Study has been completed in terms of duration but no patient has been recruited during this time” - Stop Exogenous Allergic Alveolitis (EAA) in Childhood
“After several years of recruitment only 4 patients were included. Study timelines for study completition too long. Decided to terminate trial.” - 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” - A Study of Retreatment With Brentuximab Vedotin in Subjects With Classic Hodgkin Lymphoma or CD30-expressing Peripheral T Cell Lymphoma
“Study stopped early due to low patient accrual.” - The Effect on Mucosal Healing With Pentasa Sachet in Mild to Moderate Active "Drug: Crohn's Disease"
“Study terminated due to lack of eligible patients”
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.