Autopsy report · NCT02694393
Inhaled Sodium Nitrite as an Antimicrobial for Cystic Fibrosis
Cause of deathSlow enrollment, also drug or device supply
“Protocol closed due to difficulty recruiting subjects and then expiration of investigational product and lack of a manufacturer.”
Life of this trial
- Registered 1 month before it started.
- Ran for about 6 years 5 months before it stopped.
- 4 participants enrolled.
- Results were posted on the registry 1 year 11 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1, Phase 2
- Sponsor
- Schmidhofer, Mark, MD
- Sponsor type
- University, hospital or other
- Conditions
- Cystic Fibrosis
- Interventions
- sodium nitrite
- Participants
- 4
- Sites
- 2
- Countries
- United States
Trials that died the same way
- An Efficacy and Safety Study of Golimumab in Participants With Ulcerative Colitis
“Protocol was cancelled by company based on overall efficacy, no safety concern” - Study of Heart Failure Hospitalizations After Aquapheresis Therapy Compared to Intravenous (IV) Diuretic Treatment
“Closed due to patient recruitment challenges. No interim analyses were completed; study closure was not related to any concerns about safety or futility.” - Administering Peripheral Blood Lymphocytes Transduced With a Murine T-Cell Receptor Recognizing the G12D Variant of Mutated RAS in HLA-A*11:01 Patients
“Study was closed due to lack of accrual and study outcomes overlapped with another protocol's eligibility.” - Nilotinib With Chemotherapy for the Treatment of Philadelphia Chromosome Positive Acute Lymphoblastic Leukemia
“The study was terminated due to excessive toxicity and low compliance to the protocol scheme.” - Prospective Study of Non-operative Management of SBO Without Nasogastric Tube Placement
“Study was closed due to lack of personnel for recruitment/enrollment purposes.”
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.