ClinicalTrials.Veeva

Menu

Evaluation of the Follow Me Mode of the AutoLap System - A Feasibility Study

M

M.S.T. Medical Surgery Technology

Status

Completed

Conditions

Patients Who Were Scheduled for General and Gynecological Laparoscopic Procedures

Treatments

Device: AutoLap

Study type

Interventional

Funder types

Industry

Identifiers

NCT02326870
AL-65-003

Details and patient eligibility

About

The main objectives of this study are to evaluate the performance and ease of use of the Follow me mode of the AutoLap system during general and gynecological laparoscopic procedures.

Enrollment

33 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Signed and dated Informed Consent Form (ICF).
  2. Patients over 18 years

Exclusion criteria

  1. Pregnancy
  2. Extensive adhesions that will preclude routine laparoscopic surgical approach.
  3. American Society of Anesthesiologists' (ASA) classification>2

Trial design

33 participants in 1 patient group

The AutoLap system
Experimental group
Description:
Use of the AutoLap system for controlling the laparoscope during the procedure
Treatment:
Device: AutoLap

Trial contacts and locations

4

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems