Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01929902 · ClinicalTrials.gov registry record

Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery

A clinical trial, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
20
Enrollment target

NCT01929902: Completed study, sponsored by Wake Forest University Health Sciences.

NCT01929902 is a clinical trial that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01929902 has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
20 participants
Enrollment target

Study Summary

The purpose of this study is to test the efficacy and accuracy of the Aquamantys device.

Primary Outcome

Efficacy of device will be measured based on intra-operative and post-operative complication variables: estimated blood loss, blood transfusion, complications intra-operative and post-operative.

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2013-07
Est. Completion 2014-03
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT01929902 record still lists

NCT01929902 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT01929902 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01929902 about?

NCT01929902 is a clinical study titled "Evaluation of Efficacy and Accuracy of Aquamantys Device in General Surgery". The purpose of this study is to test the efficacy and accuracy of the Aquamantys device.

What is the current status of trial NCT01929902?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2013-07. Estimated completion is 2014-03.

Who is sponsoring clinical trial NCT01929902?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01929902, the US trial registry maintained by the National Library of Medicine. NCT01929902 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.