Autopsy report · NCT05964998

Pilot Study of CBT With tDCS for Adults Being Treated for Obsessive Compulsive Disorder

“Unable to find patients willing to consent; declined for various reasoning: e.g., time commitment for the study, concerns about electrode gel in the hair, and concerns about potentially being randomized to a control group.”

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• Withdrawn before it enrolled anyone.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Withdrawn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

Na

Sponsor

Rogers Behavioral Health

Sponsor type

University, hospital or other

Conditions

Obsessive-Compulsive Disorder

Interventions

transcranial direct current stimulation; Sham transcranial direct current stimulation

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Non-pharmacological Treatments in Migraine.
  “Due to the unavailability of the subjects who gave the consent to participate to the study protocol” (57% match in meaning)
• Vanguard Knee Anterior Stabilized Versus Posterior Stabilized Bearing Study
  “Could not find interested researchers/clinicians to complete study protocol.” (57% match in meaning)
• ZEPLAST- PED: ZEro_PLASma Trial in Small Infants Undergoing Cardiac Surgery
  “The study encountered unexpected difficulties in enrolling patients due to requirements for the Informed Consent. 60% of our patients comes from abroad with only one accompanying parent. The rules of our EC require both parents to sign the consent.” (56% 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.