Autopsy report · NCT04593212
Assessment of Microcirculatory Dysfunction in Septic Shock Patients by OCTA
Cause of deathSlow enrollment, also funding or business
“Completed the case-control study (30 patients and 30 controls). The prospective cohort component was discontinued due to slow recruitment and funding constraints.”
Life of this trial
- Registered 2 years 4 months before it started.
- Ran for about 1 year 11 months before it stopped.
- 30 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Hospital da Luz, Portugal
- Sponsor type
- University, hospital or other
- Conditions
- Septic Shock
- Interventions
- Optical Coherence Tomography Angiography
- Participants
- 30
- Sites
- 1
- Countries
- Portugal
Trials that died the same way
- Depolarising Electrical Skin Stimulation in Neuropathic and Postoperative Pain
“Study was stopped due to difficulties recruting patients, at the time, 20 patients and 20 controls were included. Within last to years, only 2 patients and 2 controls could be recruted. It lookes, that the condition is to rare available.” - Safety and Pharmacokinetics of Subcutaneous Dose of IMG-007 in Healthy Participants
“Cohorts 1 and 2 were completed. Cohort 3 was cancelled because it was no longer necessary based on information from another study. No safety concerns were noted.” - Tai Chi and Wellness Education for Older Veterans
“The study was stopped after completing 2 cohorts instead of the intended 3 cohorts. This was due to logistical issues and budget-related issues (timing of being able to spend the funds).” - 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.” - A Clinical Study to Evaluate the Safety, Tolerability, PK, PD, and Efficacy of KBP-089 in Patients With T2DM
“The trial was planned to be conducted in 4 cohorts but was terminated after completion of Cohort 2 for strategic reasons due to limited PD effects.”
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.