Autopsy report · NCT04260893
Prospective Study To Assess The Safety And Effectiveness Of Tixel Treatment On Dry Eye Symptoms In Asian Patients
Cause of deathStaffing, sites or logistics
“Due to COVID19 adequate study monitoring wasn't possible by the Sponsor”
Life of this trial
- Ran for about 1 year 2 months before it stopped.
- 44 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Novoxel Ltd.
- Sponsor type
- Industry
- Conditions
- Dry Eye Syndromes; Dry Eye
- Interventions
- Tixel
- Participants
- 44
- Sites
- 1
- Countries
- Cambodia
Trials that died the same way
- Correlating the OA Knee Microenvironment to Outcomes After Regenexx-SD Treatment: A Multi-Site Study
“sponsor discontinued study-impacted by COVID” - The Georgia Latino AIDS/HIV Diagnosis and Linkage in Youth (GLADLY) Project
“The study was not able to be completed due to the COVID-19 pandemic.” - SUBA-Itraconazole Therapy for Coccidioidomycosis Refractory or Intolerant to Fluconazole
“Sponsor is not proceeding with study due to budget cuts as a result of COVID-19.” - Randomized Controlled Study Comparing Colon Evaluation With The Pure-Vu System To A Standard Colonoscopy In Patients Who Are High Risk For Inadequate Bowel Preparation
“Sponsor has terminated study due to COVID-19 related concerns” - Transgender Therapeutic Support Groups
“Study unable to be conducted due to COVID.”
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.