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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02934542
Other study ID # AL-65-006-P
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2016
Est. completion date February 2018

Study information

Verified date September 2017
Source M.S.T. Medical Surgery Technology LTD.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective of this study is to evaluate the ability to reduce the number of OR personnel required while performing the following procedures: colon resections, cholecystectomies and anti-reflux/hiatal hernia surgery with the AutoLap system compared with the standard operation.


Recruitment information / eligibility

Status Completed
Enrollment 108
Est. completion date February 2018
Est. primary completion date February 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Aged = 18 years

2. Able to provide a written informed consent

Exclusion Criteria:

1. Pregnancy

2. Obesity (BMI >35 Kg/m2)

3. Contra-indications for performing laparoscopy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
AutoLap system


Locations

Country Name City State
Netherlands Meander Medisch Centrum Amersfoort

Sponsors (1)

Lead Sponsor Collaborator
M.S.T. Medical Surgery Technology LTD.

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Success rate in performing an operation with at least one OR person less During surgery
Secondary Duration of the operation During surgery
Secondary Number of times the laparoscope is removed for cleaning During surgery
Secondary Usability evaluation Up to two days post surgery