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COMPLETED NA

A Study Assessing Circulation Around Surgical Incisions at the Time of Laparotomy Closure

NCT03408366 · View on ClinicalTrials.gov ↗

Study Summary

This study is being done to find out if Spectrum Near-Infrared (NIR) imaging with Indocyanine Green (ICG) dye can help measure blood flow around an incision before and after the surgeon closes the incision with staples or sutures. The Spectrum NIR imaging system uses a handheld camera that produces a special type of light that can help surgeons see things during surgery that are difficult to see with the naked eye, for example, cancer tissue versus healthy tissue. Spectrum NIR imaging has been approved by the Food and Drug Administration (FDA) as a tool that is widely used during surgery. ICG dye is a sterile solution that can be seen with Spectrum NIR imaging. This dye, used with Spectrum NIR imaging, allows surgeons to see blood flow to parts of the body during and after surgery. Making sure that there is enough blood flow to the surgical site helps to promote a less complicated recovery.

Conditions Studied

Interventions

  • PROCEDURE Laparotomy
  • OTHER ICG
  • OTHER Spectrum NIR imaging system

Study Locations (8)

New York

  • Memorial Sloan Kettering Commack (Consent only) — Commack
  • Memoral Sloan Kettering Westchester (Consent only) — Harrison
  • Memorial Sloan Kettering Cancer Center — New York
  • Memorial Sloan Kettering Rockville Centre (Consent only) — Rockville Centre
  • Memorial Sloan Kettering Nassau (Consent only) — Uniondale

New Jersey

  • Memoral Sloan Kettering Basking Ridge (Consent only) — Basking Ridge
  • Memoral Sloan Kettering Monmouth (Consent only) — Middletown
  • Memorial Sloan Kettering Bergen (Consent only ) — Montvale

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2018-01-15
Est. Completion 2022-08-01
Phase NA

Sponsor

Memorial Sloan Kettering Cancer Center

2,280 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03408366

The ClinicalTrials.gov registry entry for NCT03408366 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 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Memorial Sloan Kettering Cancer Center, which has 2,280 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Laparotomy appearing as the primary indexed condition, and to 3 interventions — of which Laparotomy 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: NCT03408366 reports 8 study locations spanning 2 distinct geographic areas — top geographies include New York, New Jersey. 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 NCT03408366 about?

NCT03408366 is a clinical study titled "A Study Assessing Circulation Around Surgical Incisions at the Time of Laparotomy Closure". This study is being done to find out if Spectrum Near-Infrared (NIR) imaging with Indocyanine Green (ICG) dye can help measure blood flow around an incision before and after the surgeon closes the incision with staples or sutures. The Spectrum NIR imaging system uses a handheld camera that produces...

What is the current status of trial NCT03408366?

This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2018-01-15. Estimated completion is 2022-08-01.

What conditions does trial NCT03408366 study?

This clinical trial studies the following conditions: Laparotomy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03408366?

The interventions under investigation include: Laparotomy (PROCEDURE), ICG (OTHER), Spectrum NIR imaging system (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03408366?

This trial is sponsored by Memorial Sloan Kettering Cancer Center, which has 2,280 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03408366 being conducted?

This trial has 8 study locations across New Jersey, New York. 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