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Completed

NCT Number: NCT01720966

Adhesions After Open Versus Laparoscopic Resection of Colorectal Malignancies Detected During Liver Resection

Rationale: Adhesion formation is a frequent complication after abdominal surgery. Adhesion formation might be reduced by laparoscopic surgery, however sound evidence is lacking. Colorectal surgery would be a good clinical model to investigate adhesion formation between open and laparoscopic surgery because of the adhesion formation propensity of colorectal surgery. However, a randomized controlled study to provide direct evidence is unlikely because of large numbers of patients needed for such a trial and the difficulty to check for adhesion formation at second surgery. Therefore we investigate adhesion formation after laparoscopic and open colorectal surgery for malignancy at liver surgery for metastases.

Objective: The aim of our study is to compare the incidence of adhesions after laparoscopic versus open surgery for colorectal malignancies during liver resection for colorectal metastases.

Study design: The study is designed as a prospective observational cohort study.

Study population: All consecutive, adult patients undergoing laparotomy or laparoscopy for intended liver resection or radio frequency ablation for liver metastases of a colorectal malignancy in whom inspection of the middle and lower abdomen is possible to map adhesions.

Main study parameters/endpoints:

* Primary endpoint is incidence of adhesions to the ventral abdominal wall around the site of the original incision. * Secondary endpoints are episodes of bowel obstruction between index surgery and liver surgery; total incidence of adhesions; extent of adhesions; Zühlke classification of adhesions; performance of adhesiolysis; duration of adhesiolysis; peroperative complications: enterotomy, seromuscular injury, inadvertent organ injury during adhesiolysis; postoperative complications: delayed diagnosed perforation, SAE's.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: This study is an observational study. The existence of adhesions will be assessed during laparotomy or laparoscopy for the treatment of liver metastases. The laparotomy is indicated for medical treatment and should not be enlarged solely for the assessment of adhesions nor will the operating time be influenced for this purpose.

Adhesions and peroperative complications have to be scored by the operating surgeon during or directly after surgery. The postoperative complications have to be scored during the postoperative course by the doctors on the ward. These assessments do not interfere with the treatment of the patients.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Radboud University Nijmegen Medical Center, Nijmegen, Gelderland, Netherlands

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • laparotomy or laparoscopy for intended liver resection or radio frequency ablation for colorectal metastases
  • laparoscopy or laparotomy for colorectal malignancy in history
  • age ≥18 years

Exclusion criteria

  • a history of abdominal surgery with a high risk of adhesions either before resection of the primary tumour or during the interval between resection of the primary tumour and liver resection. These high risk surgeries are:
  • Colorectal surgery
  • Ovarian surgery
  • Abdominal wall surgery
  • mental incompetence

Treatment and study plan

liver resection

Procedure

Liver resection performed for metastatic disease from colorectal carcinoma

Primary outcomes

  1. Incidence of adhesion to ventral abdominal wall

    Time frame: peroperative (1 day)

    To compare the incidence of adhesions to the ventral abdominal wall in patients undergoing laparotomy or laparoscopy for intended liver resection for colorectal metastases after open versus laparoscopic resection of the primary tumour.

Secondary outcomes

  1. Incidence of adhesions

    Time frame: peroperative (1 day)

    Total incidence of adhesions

  2. Extent of adhesions

    Time frame: peroperative (1 day)

    Extent of adhesions

  3. Adhesion Score

    Time frame: peroperative (1 day)

    Adhesion score according to Zühlke

  4. Adhesiolysis

    Time frame: peroperative (1 day)

    need to perform adhesiolysis

  5. Duration of adhesiolysis

    Time frame: peroperative (1 day)

    Duration of adhesiolysis in minutes

  6. Inadvertent bowel injury

    Time frame: peroperative (1 day)

    Inadvertent bowel injury made during operation

  7. Postoperative mobidity

    Time frame: 30 days

    Incidence of predetermined postoperative complications:

    • mortality
    • incisional wound infection
    • abdominal sepsis
    • pneumonia
    • urinary tract infection

Other outcomes

  1. Small bowel obstruction in history

    Time frame: in history (up to 5 years preceeding second operation)

    Patient has episode of small bowel obstruction in medical history

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Acronym: ALIVE

Important dates

Study start
2013
Primary completion
2015
Study completion
2015
First posted
Nov 2, 2012
Registry last updated
Nov 10, 2015

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

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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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