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NCT Number: NCT01236625

The Effect of Adhesiolysis During Elective Abdominal Surgery on Per- and Postoperative Complication, Quality of Life and Socioeconomic Costs

Official title:

LAPAD - A prospective study on the effect of adhesiolysis during elective laparotomy or laparoscopy on per- and postoperative complication, quality of life and socioeconomic costs

Background:

With improved surgical technology and ageing of the population the number of reoperations in the abdomen dramatically increases. The risk for a repeat laparotomy or laparoscopy is a high as 30% in the first ten years after a laparotomy. In over 95% of reoperations adhesiolysis is required to gain access to the abdominal cavity and operation area. Adhesiolysis significantly increases the risk for inadvertent organ damage, such as enterotomies, leading to higher morbidity, mortality and socioeconomic costs.

Purpose:

To define the impact of adhesiolysis on per- and postoperative complications, quality of life and socioeconomic costs.

Design:

Prospective observational study.

Primary outcomes:

* adhesiolysis time * inadvertent enterotomy * seromuscular injury * miscellaneous organ damage * Serious adverse events of operation (anastomotic leakage, delayed diagnosed perforation, wound infection, abdominal infection, haemorrhage, pneumonia, urinary tract infection, abscess, fistula, sepsis, death)

Secondary outcomes:

* Hospital stay * Intensive care admission * Reinterventions * In-hospital costs * Parenteral feeding * Short term readmissions (30 days) * Quality of life (Gastro- intestinal tract complaints, Short Form- 36(SF-36), DASI (Duke Activity Score Index(DASI) )

Estimated enrollment: 800 start study: 1 june 2008 Inclusion completion date: 1 june 2010 Estimated study completion date: 1 february 2011

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Radboud University Nijmegen Medical Center

Nijmegen, Gelderland, 6500HB, Netherlands

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Planned elective laparotomy or laparoscopy
  • Mentally competent
  • 18 years or older

Exclusion criteria

  • Operation cancelled
  • Bad quality of data

Treatment and study plan

Adhesiolysis

Procedure

Blunt or sharp dissection of adhesive tissue.

Primary outcomes

  1. Inadvertent Enterotomy

    Time frame: Day of surgery (one day)

    Every unintended and iatrogenic full thickness defect of the bowel.

  2. Seromuscular Injury

    Time frame: Day of surgery (one day)

    Every visible damage to the serosa, without leakage or exposure of the bowel lumen.

  3. Miscellaneous Organ Damage

    Time frame: Day of surgery (one day)

    Unintended iatrogenic damage to intra- peritoneal organs and structures other than bowel. E.g. Spleen, liver, pancreas or ureter.

  4. Serious Adverse Events

    Time frame: 30 days

    Complications marked as SAE: anastomotic leakage, delayed diagnosed perforation, wound infection, abdominal infection, haemorrhage, pneumonia, urinary tract infection, abscess, fistula, sepsis, death

  5. Adhesiolysis Time

    Time frame: Day of surgery (one day)

    Time required to dissect adhesive tissue.

Secondary outcomes

  1. Hospital stay

    Time frame: From surgery to discharge

    Number of days from surgery until discharge

  2. Reinterventions

    Time frame: 30 days after discharge

    Emergency reoperation related to a complication of initial surgery within max. 30 days after discharge.

  3. In- hospital Costs

    Time frame: From surgery to discharge

    Direct costs comprising costs from operation, stay on ward and Intesive Care Unit, medication use, diagnostics.

  4. Parenteral Feeding

    Time frame: From surgery to discharge

    Number of days that patient required parenteral feeding.

  5. Short term readmissions

    Time frame: 30 days after discharge

    Readmissions to the hospital related to complication of surgery.

  6. Quality of life

    Time frame: 6 months post surgery

    Quality of life as measured with SF-36, Gastro- intestinal tract complaints and DASI index.

Sponsors and collaborators

Lead sponsor

Radboud University Medical Center

Other

Registry information

Official study title

A Prospective Study on the Effect of Adhesiolysis During Elective Laparotomy or Laparoscopy on Per- and Postoperative Complication, Quality of Life and Socioeconomic Costs

Acronym: LAPAD

Important dates

Study start
2008
Primary completion
2011
Study completion
2011
First posted
Nov 8, 2010
Registry last updated
Nov 2, 2012

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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