Autopsy report · NCT05567692

Subjects With T2D or at Risk of T2D Cohort Follow-up

“The sponsor has temporarily suspended study due to operational constraints.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 5 months before it started.
• Suspended: paused, and may or may not restart.
• 837 participants planned (an estimate, not an actual count).

Vital statistics

Status

Suspended

Sponsor

Centre d'Etudes et de Recherche pour l'Intensification du Traitement du Diabète

Sponsor type

University, hospital or other

Conditions

Diabetes Mellitus, Type 2

Interventions

OGTT; HbA1c; Questionnaire

Participants

837 (planned, not actual)

Sites

1

Countries

France

Trials that died the same way

• An Examination of the Performance of QbMobile in Differential Diagnosis Associated With ADHD Symptoms
  “Enrollment/study activities have been temporarily suspended while the sponsor evaluates internal study priorities and resource allocation. The suspension is not related to participant safety, protocol compliance, data quality, or regulatory concerns.” (83% match in meaning)
• Premotor Cortex: A New Target for Stroke Motor Rehabilitation
  “Study was suspended pending additional funding to continue participant recruitment and was ultimately terminated in 2024.” (76% match in meaning)
• A Trial of a Botanical Drug Containing East Indian Sandalwood Oil (EISO) for the Treatment of External Genital Warts
  “Sponsor terminated study due to financial constraints.” (73% match in meaning)
• Investigation of Femoropopliteal In Situ Valve Formation With the InterVene System (INFINITE-US)
  “Project suspended by Sponsor” (73% match in meaning)
• Safety Study of Intranasal Etripamil for the Termination of Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia (PSVT). NODE-302
  “Study was stopped by the Sponsor” (72% 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.