Autopsy report · NCT04297319
The Use of Laser in the Treatment of Atrophic Vulvovaginitis
Cause of deathStaffing, sites or logistics
“This protocol was cancelled due to the COVID pandemic restrictions in our country. It was imposible to complete the recruitment of patients to achive the study objectives.”
Life of this trial
- Registered 2 months after it had already started.
- Ran for about 2 years 2 months before it stopped.
- 20 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Na
- Sponsor
- Hospital Italiano de Buenos Aires
- Sponsor type
- University, hospital or other
- Conditions
- Lasers; Atrophy of Vagina; Atrophy Vulva
- Interventions
- Laser diiodo; Laser Placebo
- Participants
- 20
- Sites
- 1
- Countries
- Argentina
Trials that died the same way
- A Phase 1/2 Study to Assess the Safety, Tolerability and Pharmacokinetics of NGM621 in Healthy Subjects, and to Assess the Safety, PK and Efficacy in Subjects With Moderate to Severe ARDS Caused by COVID-19
“Due to the rapidly changing therapeutic landscape in the COVID-19 space and an assessment of unmet medical need, Part 2 of the study was cancelled (per protocol Section 4.3). Meanwhile, Part 1 of the study was completed.” - Riociguat in Patients With Operable CTEPH Prior to Pulmonary Endarterectomy (PEA Bridging Study)
“The study was stopped due to slower than expected recruitment and the additional limitations on clinical research imposed by the COVID-19 pandemic, both of which made study completion within a reasonable timeframe appear unlikely.” - A Study of Pleiotropic Pioglitazone Effects on the Alcoholic Lung (APPEAL Study)
“Study was suspended in 2020 due to COVID-19 pandemic as a result of recruitment challenges and the inability to conduct all study procedures (e.g., bronchoscopy) per protocol. In late 2021 the decision was made to not re-open the study.” - Clinical Efficacy of Intense Pulsed Light(IPL) Procedure in Dry Eye Patient
“Due to the covid 19, patient recruiment is not going smoothly, so the study was canceled.” - Neoadjuvant and Adjuvant Nivolumab in HCC Patients Treated by Electroporation
“Because patient recruitment was affected by the COVID-19 pandemic, the study sponsor and funding partner halted enrollment at that time to meet contractual obligations”
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.