MD Anderson
Houston, Texas, 77030, United States
NCT Number: NCT05842031
To learn more about the patient experience undergoing inguinal (in the groin) lymph node procedures for penile cancer during and after surgery.
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Notify Me18 year and older
Male
Observational
Houston, Texas, 77030, United States
Objectives
Primary Objective:
To understand the lived experience of patients undergoing invasive inguinal lymph node procedures.
Secondary Objective:
To determine factors that influence decisions and improve experience for patients who need invasive inguinal lymph node procedures.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
--Patients diagnosed with penile cancer who have undergone invasive inguinal node procedures (ILND and/or DSNB) and are at least 6 months post-procedure
Exclusion criteria
Identify what interventions may be helpful in improving quality of life.
Identify what interventions may be helpful in improving patient educational needs
Identify what interventions may be helpful in improving symptom management Improve symptom management
Time frame: through study completion; an average of 1 year
Score Scale ranges (1-5)
M.D. Anderson Cancer Center
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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