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Discovering Factors in the Clinical Study Journey of Patients With OCD

P

Power Life Sciences

Status

Enrolling

Conditions

Obsessive-Compulsive Disorder
OCD

Study type

Observational

Funder types

Industry

Identifiers

NCT05881356
91191727

Details and patient eligibility

About

This research aims to collect comprehensive data on the clinical trial experience of OCD patients. Its goal is to identify the factors that limit patients' ability to join or complete a trial successfully. Clinical trial participation often favors specific demographic groups, and limited research exists on the impact of trial attributes on participation. Therefore, this study aims to analyze data from various demographic groups and identify any recurring trends that could provide valuable insights for future OCD patients.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed.
  • Participant has a diagnosis of OCD.
  • Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.

Exclusion criteria

  • Pregnant or lactating woman
  • Enrolled in another research study
  • Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial

Trial design

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Michael B Gill

Data sourced from clinicaltrials.gov

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