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

Sponsored by FluidAI Medical

About this trial

Last updated 5 years ago

Study ID

CLS0005

Status

Completed

Type

Interventional

Phase

Early Phase 1

Placebo

No

Accepting

18-75 Years
18+ Years
All
All

Trial Timing

Ended 5 years ago

What is this trial about?

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.

What are the participation requirements?

Yes

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

No

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

Locations

Location

Status