Autopsy report · NCT05339256

Sublingual Buprenorphine Through Telemedicine vs In-Person Care as Usual

“Due to a federally mandated, institution-wide pause in research activities under the institution's Federal Wide Assurance (FWA) that occurred during the timeline for this study, recruitment was never initiated and no participants were enrolled.”

The sponsor’s own words in the registry.

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• Withdrawn before it enrolled anyone.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Withdrawn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 2

Sponsor

New York State Psychiatric Institute

Sponsor type

University, hospital or other

Conditions

Opioid Use Disorder

Interventions

Buprenorphine SL; Telehealth; In-person treatment as usual

Participants

0

Trials that died the same way

• Utilizing a Promotora Model for Rural Adult Hispanics Diagnosed With Metabolic Syndrome: A Clinical Trial
  “Funding for the study was not received. No recruitment ever occurred.” (73% match in meaning)
• Comparing Concussion Education Types
  “Due to a structural change within the collaborating organization that limited implementation support, the study was not launched for recruitment, and no participants were enrolled.” (71% match in meaning)
• A Phase II Study of Ziv-aflibercept in Combination With Capecitabine/Oxaliplatin (XELOX) Chemotherapy in the Front-Line Treatment of Patients With Metastatic Colorectal Cancer
  “Funding for the study was withdrawn, no participants were ever recruited.” (71% match in meaning)
• Supervisory Neglect, Non-Accidental Trauma, Brief Intervention, and Treatment Referral
  “Study was never initiated. No IRB approval obtained, and no participants enrolled.” (70% match in meaning)
• Robotic Versus Open Comparison in the Surgical Treatment of Wide Abdominal Wall heRnias (ROCSTAR)
  “The study was not initiated and no participants were enrolled.” (70% match in meaning)

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.