NCT04245683Recruiting
Feasibility of Non-Operative Management of Rectal Cancer in a Rural Population
Source: ClinicalTrials.gov · Last updated 7 Mar 2023 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
This is an observational research study. Patients with rectal cancer can choose different courses of treatment. This study will follow these patients over the course of approximately six years, depending on their treatment. Patients will be monitored through clinic visits and survey assessments to see how they do, how they feel regarding their treatment choices, and their outcomes. The surveys will analyze the impact of the patients' treatment choices, as well as patient adherence, in a rural setting.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 50 (estimated)
- First submitted
- 27 Jan 2020
- Start date
- 1 Feb 2020
- Primary completion date
- 1 Feb 2027
- Lead sponsor
- Bassett Healthcare
- Diseases
- Colorectal cancer
- NCT number
- NCT04245683
What you commit to
- Study type: Observational
- Planned participants: 50
- From 1 Feb 2020 to the primary completion date, 1 Feb 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Patients that are not candidates for surgery
Other illness
- Patients are NOT considered eligible for this study if any of the following conditions apply:
- Patients with metastatic disease
Other
- Patients that refuse neoadjuvant treatment
Who the study is looking for
- For a patient to be considered eligible for this study, ALL of the following conditions must be met:
- Age 18 or greater
- ECOG PS 0-2
- Stage II or III, newly diagnosed, biopsy proven, rectal cancer
- No prior treatment for rectal cancer
- No prior pelvic radiotherapy
- Willing to undergo study related testing and monitoring after treatment
- Women of childbearing potential must rule out pregnancy within 2 weeks prior to registration with a blood test or urine study
- Women must not be pregnant or breastfeeding
- Able to provide informed consent
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Bassett Healthcare Network Coordinator of this site? Confirm its status | Cooperstown | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.