Understanding patient experiences with inguinal lymph node procedures for penile cancer
Assessment of Patient Experience and Needs for Patients Undergoing Invasive Inguinal Lymph Node Procedures for Penile Cancer
This study is trying to learn about the experiences of patients who have had surgery on their lymph nodes for penile cancer to see how it affects their lives and how to improve care for future patients.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20 (estimated) |
| Ages | 18 Years and up |
| Sex | Male |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Trial ID | NCT05842031 on ClinicalTrials.gov |
What this trial studies
This observational study aims to gather insights into the experiences of patients who have undergone invasive inguinal lymph node procedures for penile cancer. It focuses on understanding their lived experiences during and after surgery, as well as identifying factors that influence their decisions and overall satisfaction. The study employs quality of life questionnaires and explores patient educational needs and symptom management to enhance the patient experience. By collecting this data, the study seeks to improve care for future patients undergoing similar procedures.
Who should consider this trial
Good fit: Ideal candidates for this study are patients diagnosed with penile cancer who have undergone invasive inguinal lymph node procedures and are at least six months post-procedure.
Not a fit: Patients who are under 18 years of age, have not undergone the specified surgical procedures, or are non-English speakers may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved patient care and support for individuals undergoing invasive procedures for penile cancer.
How similar studies have performed: While this study focuses on patient experiences, similar studies in other cancer types have shown success in improving patient care and outcomes.
Eligibility criteria
Show full inclusion / exclusion criteria
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: * Patient's ≤18 years of age * Patients who have not undergone invasive surgical procedures involving the inguinal lymph nodes * Non-English-speaking patients For interviews: people who are physically and/or cognitively incapable of participating in a 60minute telephone interview as determined by a clinical provider or the patient.
Where this trial is running
Houston, Texas
- MD Anderson — Houston, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Curtis Pettaway, BS, MD — MD Anderson
- Study coordinator: Curtis Pettaway, BS, MD
- Email: cpettawa@mdanderson.org
- Phone: (713) 792-3250
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.