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COMPLETED NA

A Study Assessing the Safety and Utility of PINPOINT® Near Infrared Fluorescence Imaging in the Identification of Lymph Nodes in Patients With Uterine and Cervical Malignancies Who Are Undergoing Lymph Node Mapping

NCT02209532 · View on ClinicalTrials.gov ↗

Study Summary

This is a randomized, prospective, open label, multicenter study to assess the safety and utility of PINPOINT® Near Infrared Fluorescence Imaging (PINPOINT) in identification of lymph nodes (LN) in patients with uterine and cervical malignancies who are undergoing LN mapping.

Interventions

  • DEVICE PINPOINT

Study Locations (8)

California

  • O'Connor Hospital — San Jose

Florida

  • Lee Memorial Hospital — Fort Myers

New York

  • Memorial Sloan Kettering — New York

North Carolina

  • Duke Cancer Institute — Durham

Texas

  • MD Anderson Cancer Center — Houston

Ontario

  • Sunnybrook Health Science Centre — Toronto

Quebec

  • CHU de Québec - Université Laval — Québec

Other

  • Hospital HIMA San Pablo — Caguas

Trial Details

FieldValue
Enrollment Target 180 participants
Start Date 2015-12
Est. Completion 2017-06
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02209532

The ClinicalTrials.gov registry entry for NCT02209532 describes a study currently listed as completed. 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 180 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novadaq Technologies ULC, now a part of Stryker, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 3 conditions, with Endometrial Cancer appearing as the primary indexed condition, and to 1 intervention — of which PINPOINT 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: NCT02209532 reports 8 study locations spanning 8 distinct geographic areas — top geographies include California, Florida, New York. 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 NCT02209532 about?

NCT02209532 is a clinical study titled "A Study Assessing the Safety and Utility of PINPOINT® Near Infrared Fluorescence Imaging in the Identification of Lymph Nodes in Patients With Uterine and Cervical Malignancies Who Are Undergoing Lymph Node Mapping". This is a randomized, prospective, open label, multicenter study to assess the safety and utility of PINPOINT® Near Infrared Fluorescence Imaging (PINPOINT) in identification of lymph nodes (LN) in patients with uterine and cervical malignancies who are undergoing LN mapping.

What is the current status of trial NCT02209532?

This trial is currently completed. It is a NA study. The enrollment target is 180 participants. The study started on 2015-12. Estimated completion is 2017-06.

What conditions does trial NCT02209532 study?

This clinical trial studies the following conditions: Endometrial Cancer, Cervical Cancer, Uterine Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02209532?

The interventions under investigation include: PINPOINT (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02209532?

This trial is sponsored by Novadaq Technologies ULC, now a part of Stryker, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02209532 being conducted?

This trial has 8 study locations across California, Florida, New York, North Carolina, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial