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Clinical Trials/NCT01521871
NCT01521871
Completed
Phase 4

A Prospective, Randomised Study on Tissue Glue (Cyanoacrylate) Versus Conventional Suture for Skin Closure in Laparoscopic Living Donor Nephrectomy

Oslo University Hospital1 site in 1 country64 target enrollmentJanuary 2012

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Skin Closure of Surgical Incisions by Tissue Glue vs Suture
Sponsor
Oslo University Hospital
Enrollment
64
Locations
1
Primary Endpoint
Wound Healing by Numerical Scales for Secretion Postoperative Day 2.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

By means of a prospective, randomised trial the investigators want to examine skin closure in living donors - subjected to laparoscopic, hand-assisted nephrectomy - by tissue glue (Cyanoacrylate (Liquiband)) versus conventional, intracutaneous suture and dressing (1 : 1; 30 + 30 donors).

Study hypothesis: (i) Latest generation tissue glue (Cyanoacrylate (Liquiband)) is at least as good as conventional suture regarding wound healing/complications. (ii) Peroperatively, tissue glue is faster than conventional suture.

Detailed Description

At Oslo University Hospital Rikshospitalet, the principal investigator have since 1998 been involved in developing minimally invasive techniques for living donor nephrectomy (LDN). Since 2009 all LDN's have been performed by laparoscopic, hand-assisted technique; by means of 'handport' and 3 laparoscopic ports (5/12 mm). The investigators consider use of tissue glue instead of suture as another small step towards less invasive surgery. Since 2000 there has been many reports, and even Cochrane reviews on the use/safety of tissue glue for skin closure. However, very few randomised studies have been performed with the latest generation tissue glue; Cyanoacrylate, with a critical mixture of octyl-:butyl-acrylate. And in Norway there has been no research in this field. On this basis, the investigators intend to examine skin closure in living donors, a very healthy/homogenous study population, subjected to laparoscopic, hand-assisted nephrectomy, by a prospective, randomised trial: Tissue glue (Cyanoacrylate (Liquiband)) versus conventional, intracutaneous suture and dressing (1 : 1; 30 + 30 donors). Primarily, the investigators will examine wound healing/complications by wound observation at postop. days 2 + 4 + 'at departure', with numerical scales for secretion, gaps, edema, rubor - as well as infection/bacteriology and complications/ reinterventions. In addition, the donors' self-satisfaction with the wound handling will be registered. Furthermore, the investigators will look at time consumption during surgery, price, stay in hospital and cosmesis judged at 2-3 months postoperatively.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
February 2013
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Oslo University Hospital
Responsible Party
Principal Investigator
Principal Investigator

Ole Morten Øyen

Principal Investigator

Oslo University Hospital

Eligibility Criteria

Inclusion Criteria

  • Living kidney donor with informed consent
  • Approved comprehensive work-up/evaluation at local hospital

Exclusion Criteria

  • Allergy towards acrylate or similar chemicals
  • Unable to communicate in norwegian language

Outcomes

Primary Outcomes

Wound Healing by Numerical Scales for Secretion Postoperative Day 2.

Time Frame: Postop. day 2

The evaluation is performed by the use of a previously set numerical scale for secretion ((0-3; 0: totally dry - 3: continuous secretion). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Secretion Postoperative Day 4.

Time Frame: Postop. day 4

The evaluation is performed by the use of a previously set numerical scale for secretion ((0-3; 0: totally dry - 3: continuous secretion). Both arms/groups are evaluated day 4 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Secretion at Discharge From Hospital.

Time Frame: At departure from Surgical Dep. to the patients home, usually at postop. day 4, 5, 6 or 7

The evaluation is performed by the use of a previously set numerical scale for secretion ((0-3; 0: totally dry - 3: continuous secretion). Both arms/groups are evaluated day 4 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Oedema Postoperative Day 2.

Time Frame: Postop. day 2

The evaluation is performed by the use of a previously set numerical scale for oedema (0-1; 0: no elevation - 1: oedema causing \> 2 mm elevation). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Oedema Postoperative Day 4.

Time Frame: Postop. day 4

The evaluation is performed by the use of a previously set numerical scale for oedema (0-1; 0: no elevation - 1: oedema causing \> 2 mm elevation). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Oedema at Discharge From Hospital.

Time Frame: At departure from Surgical Dep. to the patients home, usually at postop. day 4, 5, 6 or 7

The evaluation is performed by the use of a previously set numerical scale for oedema (0-1; 0: no elevation - 1: oedema causing \> 2 mm elevation). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Blisters Postoperative Day 2.

Time Frame: At postop. day 2 (2 days after kidney donation)

The evaluation is performed by the use of a previously set numerical scale for blisters (0: none - 3: abundant). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Blisters Postoperative Day 4.

Time Frame: At postop. day 4 (4 days after kidney donation)

The evaluation is performed by the use of a previously set numerical scale for blisters (0: none - 3: abundant). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Blisters at Discharge From Hospital.

Time Frame: At departure from Surgical Dep. to the patients home, usually at postop. day 4, 5, 6 or 7

The evaluation is performed by the use of a previously set numerical scale for blisters (0: none - 3: abundant). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Gaps Postoperative Day 2.

Time Frame: Postop. day 2

The evaluation is performed by the use of a previously set numerical scale for gaps (0: no gap - 3: need for resuture/strips). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Gaps Postoperative Day 4.

Time Frame: Postop. day 4

The evaluation is performed by the use of a previously set numerical scale for gaps (0: no gap - 3: need for resuture/strips). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Rubor Postoperative Day 2.

Time Frame: At postoperative day 2 (2 days after kidney donation)

The evaluation is performed by the use of a previously set numerical scale for rubor (0-3; 0: pale, 3: typically infectious). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Rubor Postoperative Day 4.

Time Frame: At postop. day 4 (4 days after kidney donation)

The evaluation is performed by the use of a previously set numerical scale for rubor (0-3; 0: pale, 3: typically infectious). Both arms/groups are evaluated day 4 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Rubor at Discharge From Hospital.

Time Frame: At departure from Surgical Dep. to the patients home, usually at postop. day 4, 5, 6 or 7

The evaluation is performed by the use of a previously set numerical scale for rubor (0-3; 0: pale, 3: typically infectious). Both arms/groups are evaluated day 4 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

Wound Healing by Numerical Scales for Gaps at Discharge From Hospital.

Time Frame: At departure from Surgical Dep. to the patients home, usually at postop. day 4, 5, 6 or 7

The evaluation is performed by the use of a previously set numerical scale for gaps (0: no gap - 3: need for resuture/strips). Both arms/groups are evaluated day 2 postoperatively to measure any difference between the two skin closure methods. A high score is used as indicator of traumaticity towards the skin and a higher potential for wound infection.

TIme Consumption

Time Frame: The specific time required for skin closure (tissue adhesive versus suture) was recorded, counted from initial application of adhesive/intracutaneous suture until final dressing.

The specific time required for skin closure (tissue adhesive versus suture) was recorded, counted from initial application of adhesive/intracutaneous suture until final dressing.

Patients´Self Satisfaction.

Time Frame: These data were collected at the day of discharge from hospital (postoperative day 4-8).

The patients' self-satisfaction was evaluated by means of a questionnaire rating the following 3 domains on a numerical (1-5) scale: * Total satisfaction regarding wound healing/wound care. 1 (satisfied) to 5 (dissatisfied) * Satisfaction regarding wound discomfort; pain, itching, paresthesia, pressure etc. 1 (almost no discomfort) to 5 (lot of discomfort) * Satisfaction regarding wound care; suppleness, practicability versus mobilization, showering etc. 1 (almost no practical challenges) to 5 (lot of practical challenges) Patients' Self Satisfaction score was the sum of three domains, ranges from 3 (completely satisfied) to 15 (completely dissatisfied). These data were collected at the day of discharge, with guidance from two interviewers.

Study Sites (1)

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