Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Use of a Pre-Surgical Toolkit in Improving Surgical Care and Outcomes in Older Participants With Cancer
NCT03857620 · View on ClinicalTrials.gov ↗
Study Summary
This trial studies how well the use of a pre-surgical toolkit (OPTI-Surg) works in improving surgical care and outcomes in older participants with cancer. In many elderly patients, surgery can greatly affect physical condition and the ability to return to pre-surgery levels of physical functioning. Providing pre-surgical recommendations may help improve participants' recovery rate and functioning after surgery.
Conditions Studied
Interventions
- OTHER Questionnaire Administration
- OTHER Best Practice
- OTHER Informational Intervention
- OTHER Informational Intervention with Coaching
Study Locations (20)
Minnesota
- Fairview Southdale Hospital — Edina
- Hennepin County Medical Center — Minneapolis
- North Memorial Medical Health Center — Robbinsdale
Georgia
- Augusta University Medical Center — Augusta
- Memorial Health University Medical Center — Savannah
Illinois
- Advocate Christ Medical Center — Oak Lawn
- Carle Cancer Center — Urbana
Iowa
- Iowa Methodist Medical Center — Des Moines
- Mercy Medical Center - Des Moines — Des Moines
Kansas
- University of Kansas Cancer Center — Kansas City
- University of Kansas Hospital-Westwood Cancer Center — Westwood
Louisiana
- LSU Healthcare Network / Metairie Multi-Specialty Clinic — Metairie
- Louisiana State University Health Science Center — New Orleans
Michigan
- Saint Joseph Mercy Hospital — Ann Arbor
- Spectrum Health at Butterworth Campus — Grand Rapids
Delaware
- Helen F Graham Cancer Center — Newark
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 325 participants |
| Start Date | 2019-07-24 |
| Est. Completion | 2025-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03857620
The ClinicalTrials.gov registry entry for NCT03857620 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 325 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alliance for Clinical Trials in Oncology, which has 147 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Malignant Neoplasm appearing as the primary indexed condition, and to 4 interventions — of which Questionnaire Administration is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03857620 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Minnesota, Georgia, Illinois. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03857620 about?
NCT03857620 is a clinical study titled "Use of a Pre-Surgical Toolkit in Improving Surgical Care and Outcomes in Older Participants With Cancer". This trial studies how well the use of a pre-surgical toolkit (OPTI-Surg) works in improving surgical care and outcomes in older participants with cancer. In many elderly patients, surgery can greatly affect physical condition and the ability to return to pre-surgery levels of physical functioning. ...
What is the current status of trial NCT03857620?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 325 participants. The study started on 2019-07-24. Estimated completion is 2025-10.
What conditions does trial NCT03857620 study?
This clinical trial studies the following conditions: Malignant Neoplasm, Carcinoma, Surgical Procedure, Unspecified, Health Care Provider. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03857620?
The interventions under investigation include: Questionnaire Administration (OTHER), Best Practice (OTHER), Informational Intervention (OTHER), Informational Intervention with Coaching (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03857620?
This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 147 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03857620 being conducted?
This trial has 20 study locations across Delaware, District of Columbia, Georgia, Hawaii, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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