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Evaluating Factors In Study Experiences of Lymphedema Patients

P

Power Life Sciences

Status

Not yet enrolling

Conditions

Lymphedema

Study type

Observational

Funder types

Industry

Identifiers

NCT05948345
83474689

Details and patient eligibility

About

The study intends to investigate the personal experiences of lymphedema patients who take part in a separate clinical trial including a specific medication intervention. The major focus will be on closely following individuals' rates of trial completion and withdrawal.

The data collected from this study will help improve future outcomes for all lymphedema patients as well as those in under-represented demographic groups.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients diagnosed with lymphedema
  • Aged ≥ 18 years old and ability to provide written informed consent obtained prior to participation in the study and any related procedures being performed
  • Subjects willing and able to comply with the protocol for the duration of the study including undergoing treatment and scheduled visits and examination.

Exclusion criteria

  • Refusal of consent
  • Women of childbearing potential without a negative pregnancy test; or women who are lactating.
  • Any serious and/or unstable pre-existing medical disorders

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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