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Completed

NCT Number: NCT02459405

Decreasing Leak Rate in Colorectal Surgery Using Near Infra-red (NIR) Imaging

Anastomotic leak is a devastating complication of colorectal surgery. There is no widespread means of assessing the viability of a laparoscopic anastomosis. The investigators described recently the feasibility of microvascularisation assessment with near-infra red technology (NIR).

The aim of this study is to look at the implementation of this technique in a wider prospective series of patients undergoing colorectal resection.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Dublin University College, department of colorectal surgery, Dublin, Ireland

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About this study

Multicentric prospective study of 260 consecutive patients undergoing colonic resection and being assessed during the course of surgery for microvascularisation.

After vessel division and after colorectal anastomosis, indocyanine green (2.5mg/ml) is injected intravenously and anastomotic microvascularisation assessed with the PinPoint NIR system (Novadaq, Vancouver, Canada).

Study primary endpoint is the anastomotic leak rate Secondary endpoint are peroperative and post-operative complications according to the Clavien Dindo scale, time of the procedure and time to record a signal as well as any change of the procedure.

This study will be performed on 3 different sites Geneva, Oxford and Dublin University Hospitals

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participant is willing and able to give informed consent for participation in the study.
  • Participant willing and able to comply with the study procedures.
  • Diagnosed with required colon or rectal neoplasia requiring surgical excision by either laparoscopic or open surgery.
  • A negative pregnancy test for women of childbearing potential prior to surgery
  • Able (in the Investigators opinion) and willing to comply with all study requirements

Exclusion criteria

  • Female participant who is pregnant, lactating or planning pregnancy during the course of the study.
  • Allergy to Indocyanine green.
  • Participant who is undergoing purely palliative surgery or who is terminally ill
  • Subject has other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the study, or may influence the result of the study, or the participant's ability to participate in the study.

Treatment and study plan

NIR anastomotic perfusion assessment

Procedure

Patient will have their anastomosis assessed by near infrared technology after indocyanine green has been injected i.v. The procedure will be repeated twice, once before the anastomosis and the second time after the anastomosis has been performed.

Other names: Indocyanine assessment of anastomotic microvascularisation

Near Infrared Camera

Device

Use of the Pinpoint laparoscopic scope (Novadaq, Vancouver, Canada) after injection of indocyanine green

Other names: Pinpoint evaluation

Primary outcomes

  1. Anastomotic leak rate

    Time frame: first 30 days

    anastomotic leak rate at 30 post operative days

Secondary outcomes

  1. Time to perform the near infrared procedure

    Time frame: during surgery

    measured added time to the procedure

  2. Time to get a near infrared signal

    Time frame: during surgery

    Time to see a signal during surgery

  3. complication rate

    Time frame: 30 days

    according to Clavien Dindo classification

  4. Mortality

    Time frame: 30 days

    30 days mortality

  5. Alteration of the course of surgery due to insufficient vascularisation

    Time frame: during surgery

    If the vascularisation is insufficient during the surgery, the investigators can change the course of the surgery he is performing. For example, it could lead to a second resection to obtain well vascularized tissue for the anastomosis. Any alteration of the regular course of surgery for the safety of the patient is reported. The number of patient requiring an alteration of the course of surgery will be recorded.

Sponsors and collaborators

Lead sponsor

University Hospital, Geneva

Other

Collaborators

  • Oxford University Hospitals NHS Trust
  • University College Dublin

Registry information

Official study title

Decreasing Leak Rate in Colorectal Surgery Using Near Infra-red (NIR) Imaging: a Multicentric Prospective Phase II Study

Important dates

Study start
2013
Primary completion
2016
Study completion
2016
First posted
Jun 2, 2015
Registry last updated
May 4, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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