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Feasibility of Stereotactic Navigation in Laparoscopic Surgery for Colorectal Cancer (PELVINAV)

Primary Purpose

Colorectal Cancer

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Intraoperative acquisition (robotic c-Arm) of images
Sponsored by
IHU Strasbourg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Colorectal Cancer focused on measuring stereotactic navigation, colorectal cancer, laparoscopy, transanal surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patient is over 18 years old
  2. Patient presents with cancer
  3. Patient has no contraindication to anesthesia and surgical resection
  4. Patient able to receive and understand information about the study and give written informed consent
  5. Patient (s) affiliated to the national social security system.

Exclusion Criteria:

  1. Patient operated on urgently.
  2. Pregnant or lactating patient
  3. Patient in an exclusion period (determined by previous or current study).
  4. Patient under the protection of justice.
  5. Patient under guardianship or curatorship.

Sites / Locations

  • Service de Chirurgie Digestive et Endocrinienne, NHCRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

PREOP

PEROP

Arm Description

Navigation without intraoperative acquisition of images: Use of conventional preoperative images (CT-MRI) to establish intraoperative navigation.

Navigation with intraoperative acquisition of images: Intraoperative acquisition (robotic c-Arm) of images to establish intraoperative navigation.

Outcomes

Primary Outcome Measures

Accuracy of Surgical stereotactic navigation defined as the distance, in millimetres, between the position of the surgical landmark and the position determined by the navigation system
Measurement of "accuracy" of surgical navigation defined as the distance measured between the position of "surgical" previously defined anatomical landmarks, pointed with a surgical instrument tracked by the navigation system, and corresponding location of the instrument in the navigation image. A distance equal to or less than 4 mm between the two locations will be considered as an optimum accuracy.

Secondary Outcome Measures

Comparison, in millimeters, of the surgical navigation "accuracy" (as defined in the primary outcome) with or without intraoperative images acquisition
Usefulness of intraoperative images acquisition for the registration process of the navigation system by comparing accuracy of surgical navigation (in mm) with or without intraoperative images acquisition
Difference, in millimetres, between the alignment of the geometric position of the markers in the image space and the actual physical space for stereotaxic navigation
Measurement of "registration error" during surgical navigation defined as the difference between the alignment of the geometric position of the markers in the image space and the actual physical space, with or without intraoperative images acquisition. An error of 2 mm during the recording process will be considered as the optimal parameter
Measurement of the overall operating time (in minutes) with and without intraoperative images acquisition
Evaluation of the impact of the introduction of surgical navigation on the operating time. The measurement of the overall operating time (expressed in minutes), associated with surgical navigation
Measurement of the level of radiation exposure to ionizing factors with and without intraoperative images acquisition
Evaluation of the impact of the introduction of surgical navigation on the exposure of the patient to ionizing radiation, measured with Dose Length Product (DLP) and expressed in mGy * cm
Number of intra and/or postoperative complication
Evaluation of the impact of the introduction of surgical navigation on the incidence of intra- and / or postoperative complications associated with surgical navigation

Full Information

First Posted
January 14, 2019
Last Updated
August 18, 2022
Sponsor
IHU Strasbourg
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1. Study Identification

Unique Protocol Identification Number
NCT03806244
Brief Title
Feasibility of Stereotactic Navigation in Laparoscopic Surgery for Colorectal Cancer
Acronym
PELVINAV
Official Title
Prospective Study of the Feasibility of Stereotactic Navigation in Laparoscopic Surgery for Colorectal Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
August 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 17, 2019 (Actual)
Primary Completion Date
April 2023 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
IHU Strasbourg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
To evaluate the feasibility and precision of stereotaxic navigation in laparoscopic surgery for colorectal cancer.
Detailed Description
In minimally invasive surgery, the proper identification of the correct anatomical planes can be difficult due to a lack of tactile feedback and the inability to manually palpate the organ prior to resection. Although this can be minimized by careful preoperative planning, the information that can be obtained by images is also of limited utility. Conventional imaging, such as magnetic resonance imaging (MRI) and computed tomography (CT-scan), can provide a detailed view of 2D or 3D internal anatomical structures. However, during surgery, surgeons still have to use their subjective interpretation to translate this information into three-dimensional spatial relationships (ie the patient's actual volume). For this reason, in order to perform adequate resection and avoid injury, the surgeon must constantly infer what is the actual location of the anatomical structures and what is the position of the surgical instruments in relation thereto. The proposed study aims to evaluate the feasibility of surgical navigation in patients with colorectal cancer (sigmoid rectum-right-left rectum) and measure its performance in the perspective of a more specific application to rectal cancer approached laparoscopically through the abdomen and / or the anus. The study is proposed to patients with cancer because the measurement of accuracy will be done on predefined anatomical points that will be detectable in the surgical field after oncologic dissection. Benign pathologies do not require this type of extensive dissection and the application of navigation would imply additional risks for patients. Surgical navigation will be performed on the basis of preoperative images or intraoperative images.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
stereotactic navigation, colorectal cancer, laparoscopy, transanal surgery

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
PREOP
Arm Type
No Intervention
Arm Description
Navigation without intraoperative acquisition of images: Use of conventional preoperative images (CT-MRI) to establish intraoperative navigation.
Arm Title
PEROP
Arm Type
Experimental
Arm Description
Navigation with intraoperative acquisition of images: Intraoperative acquisition (robotic c-Arm) of images to establish intraoperative navigation.
Intervention Type
Other
Intervention Name(s)
Intraoperative acquisition (robotic c-Arm) of images
Intervention Description
Conventional laparoscopic colorectal oncologic resection is performed. During the procedure, the operator will identify previously defined anatomical landmarks, point them with an instrument tracked by the navigation system and the accuracy of the stereotactic navigation system will be calculated by comparing the "surgical" anatomical point and its correspondent on the images of the navigation platform.
Primary Outcome Measure Information:
Title
Accuracy of Surgical stereotactic navigation defined as the distance, in millimetres, between the position of the surgical landmark and the position determined by the navigation system
Description
Measurement of "accuracy" of surgical navigation defined as the distance measured between the position of "surgical" previously defined anatomical landmarks, pointed with a surgical instrument tracked by the navigation system, and corresponding location of the instrument in the navigation image. A distance equal to or less than 4 mm between the two locations will be considered as an optimum accuracy.
Time Frame
up to 7 days post procedure
Secondary Outcome Measure Information:
Title
Comparison, in millimeters, of the surgical navigation "accuracy" (as defined in the primary outcome) with or without intraoperative images acquisition
Description
Usefulness of intraoperative images acquisition for the registration process of the navigation system by comparing accuracy of surgical navigation (in mm) with or without intraoperative images acquisition
Time Frame
up to 7 days post procedure
Title
Difference, in millimetres, between the alignment of the geometric position of the markers in the image space and the actual physical space for stereotaxic navigation
Description
Measurement of "registration error" during surgical navigation defined as the difference between the alignment of the geometric position of the markers in the image space and the actual physical space, with or without intraoperative images acquisition. An error of 2 mm during the recording process will be considered as the optimal parameter
Time Frame
up to 7 days post procedure
Title
Measurement of the overall operating time (in minutes) with and without intraoperative images acquisition
Description
Evaluation of the impact of the introduction of surgical navigation on the operating time. The measurement of the overall operating time (expressed in minutes), associated with surgical navigation
Time Frame
up to 30 days post procedure
Title
Measurement of the level of radiation exposure to ionizing factors with and without intraoperative images acquisition
Description
Evaluation of the impact of the introduction of surgical navigation on the exposure of the patient to ionizing radiation, measured with Dose Length Product (DLP) and expressed in mGy * cm
Time Frame
up to 30 days post procedure
Title
Number of intra and/or postoperative complication
Description
Evaluation of the impact of the introduction of surgical navigation on the incidence of intra- and / or postoperative complications associated with surgical navigation
Time Frame
up to 30 days post procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is over 18 years old Patient presents with cancer Patient has no contraindication to anesthesia and surgical resection Patient able to receive and understand information about the study and give written informed consent Patient (s) affiliated to the national social security system. Exclusion Criteria: Patient operated on urgently. Pregnant or lactating patient Patient in an exclusion period (determined by previous or current study). Patient under the protection of justice. Patient under guardianship or curatorship.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Armelle Takeda, PhD
Phone
+33(0)390413608
Email
armelle.takeda@chru-strasbourg.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Bernard Dallemagne, MD
Email
bernard.dallemagne@ircad.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Didier Mutter, MD, PhD
Organizational Affiliation
Service Chirurgie Digestive et Endocrinienne, Nouvel Hôpital Civil de Strasbourg
Official's Role
Principal Investigator
Facility Information:
Facility Name
Service de Chirurgie Digestive et Endocrinienne, NHC
City
Strasbourg
ZIP/Postal Code
67 091
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Didier Mutter, MD, PhD
Phone
+33(0)3 69 55 05 53
Email
didier.mutter@chru-strasbourg.fr

12. IPD Sharing Statement

Plan to Share IPD
No
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http://adsabs.harvard.edu/abs/2016SPIE.9786E..2LN
Description
Image-guided navigation surgery for pelvic malignancies using electromagnetic tracking - Proceedings of the SPIE
URL
https://core.ac.uk/download/pdf/82477249.pdf
Description
The use of image guided navigation tracking systems for endoscopic sinus surgery and skull base surgery : a review
URL
https://doi.org/10.1053/j.oto.2017.09.010
Description
Stereotactic Navigation in Complex Spinal Surgery: Tips and Tricks

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Feasibility of Stereotactic Navigation in Laparoscopic Surgery for Colorectal Cancer

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