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Assessing Medical Trial Experiences of Hairy Cell Leukemia Patients

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Hairy Cell Leukemia

Study type

Observational

Funder types

Industry

Identifiers

NCT05859932
81405664

Details and patient eligibility

About

The percentages of participants in clinical studies haven't always been perfectly representative of a particular group.

This research examines the variables that affect a patient's choice to enroll in, discontinue participation in, or resume participation in a clinical trial for hairy cell leukemia.

It will also try to analyze data from the perspective of different demographic groups to check for recurring trends which might yield insights for the sake of hairy cell leukemia studies.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged ≥ 18 years old
  • Ability to understand and the willingness to sign a written informed consent document.
  • Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.

Exclusion criteria

  • Is pregnant, breastfeeding or expecting to conceive within the projected duration of the study
  • Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
  • Patients with any significant history of non-compliance to medical regimens or with inability to grant a reliable informed consent.

Trial design

Trial documents
1

Trial contacts and locations

0

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Central trial contact

Michael B Gill

Data sourced from clinicaltrials.gov

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