Status:

TERMINATED

Characterization of Treatment Responses in Lymphedema

Lead Sponsor:

Stanford University

Conditions:

Lymphedema

Eligibility:

All Genders

18-75 years

Brief Summary

This study is designed to investigate the treatment response of lymphedema, of the upper or lower extremity, during clinical, pharmacologic treatment of lymphedema with oral ketoprofen. Correlation of...

Detailed Description

Patients presenting to the Investigator's Clinic for evaluation and treatment of (upper or lower extremity) lymphedema, will be assessed for their suitability (of low risk) for medical treatment with ...

Eligibility Criteria

Inclusion

  • Participants with a history of acquired lymphedema
  • Stage 1, 2, or 3
  • 18-75 years
  • Clinical use of ketoprofen for lymphedema

Exclusion

  • Active cancer, infection, bleeding tendency, inflammatory disease and/or taking anti-inflammatory or anti-leukotriene medication will be excluded.
  • Pregnant or lactating females
  • Inability to take ketoprofen (contra-indicated, e.g patients with known CV, GI, renal, hepatic disease).
  • Other severe acute or chronic medical or psychiatric condition or laboratory abnormality that may increase the risk associated with study participation, may interfere with interpretation of study results, and in the judgement of the investigator, would make the participation inappropriate for entry into this study.

Key Trial Info

Start Date :

June 21 2019

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

August 31 2023

Estimated Enrollment :

2 Patients enrolled

Trial Details

Trial ID

NCT03783715

Start Date

June 21 2019

End Date

August 31 2023

Last Update

October 10 2023

Active Locations (1)

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Stanford University

Stanford, California, United States, 94305