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OpenTrials
Completed

NCT Number: NCT04253028

Use of NERv's Inline Device as an Early Diagnostic Method for Anastomotic Leak.

NERv's early feasibility clinical trial is a first-in-human, multi-center, pre-market, non-randomized clinical trial intended to evaluate the safety and collect preliminary data necessary for the detection of clinical post-operative anastomotic/intraperitoneal leakages.

NERv's Inline Device attaches to existing catheters or peritoneal drains that are currently being used in the medical industry. This allows the device to measure the pH and conductance of intraperitoneal fluids that typically get drained through peritoneal drains.

The purpose of NERv's feasibility clinical trial is to collect pH and conductance readings by analyzing peritoneal drainage fluid. Upon analyzing data collected from NERv's Inline Device a clinical model of pH and conductance will be created. The clinical model can then be used to determine if a complication is developing. For instance, boundaries (reading thresholds) can be established where if the signal goes outside the boundaries a complication could be identified. Specifically the ability to detect a post-operative complication known as anastomotic leakage; which is a dreaded complication associated with abdominal surgeries; will be the main focus of the study.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

Assiut University Hospital, Cairo, Egypt

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years - male or female
  • Subject understands and has voluntarily signed and dated Informed Consent Form (ICF)
  • Subjects must be willing to comply with trial requirements
  • Subject has a peritoneal drain attached post-surgery

Exclusion criteria

  • Plans that the subject will be discharged less than 8 hours post-surgery
  • Involvement in the planning and conduct of the clinical investigation
  • Subject is participating in another investigational drug or device study which would interfere with the endpoints and follow-ups of this study
  • Subject is consuming steroid or anti-inflammatory medication

Treatment and study plan

NERv's Inline Device

Device

NERv's Inline Device attaches to existing catheters or peritoneal drains that are currently being used in the medical industry. This allows the device to measure the pH and conductance of intraperitoneal fluids that typically get drained through peritoneal drains.

Primary outcomes

  1. Change in pH of Peritoneal Fluid

    Time frame: A clinical model of change in pH over time will be established once the study is completed (up to 28 weeks).

    NERv's Inline Device will be collecting continuous pH measurements of fluid that travels across the peritoneal drain of bariatric surgery patients.

  2. Change in Conductance of Peritoneal Fluid

    Time frame: A clinical model of change in conductance over time will be established once the study is completed (up to 28 weeks).

    NERv's Inline Device will be collecting continuous conductance measurements of fluid that travels across the peritoneal drain of bariatric surgery patients.

  3. Change in Temperature of Peritoneal Fluid

    Time frame: A clinical model of change in temperature over time will be established once the study is completed (up to 28 weeks).

    NERv's Inline Device will be collecting continuous temperature measurements of fluid that travels across the peritoneal drain of bariatric surgery patients.

  4. Number of Subjects with Device Related Adverse Events

    Time frame: The number of device related will be established once the study is completed (up to 28 weeks).

    an adverse event assesmtent will be performed in accordance to ISO 14155 standards to determine the number of device related adverse events.

Secondary outcomes

  1. Investigator and Subject Feedback on Device's Ease of Use and Comfort level

    Time frame: Overall comfort level and ease of use will be established once the study is completed (up to 28 weeks).

    Ease of use and comfort levels will be evaluated by collecting responses to a questionnaire that will be filled out by both the investigator/nurse and the subject.

Sponsors and collaborators

Lead sponsor

FluidAI Medical

Industry

Collaborators

  • Unity Health Toronto

Registry information

Official study title

Use of NERv's Inline Device for the Continuous Monitoring of pH and Conductance Measurements as an Early Diagnostic Method for Anastomotic Leak.

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Feb 5, 2020
Registry last updated
Aug 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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