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Hand-assisted Laparoscopic Donor Nephrectomy Periumbilical Versus Pfannenstiel Incision (HAPERPACT)

Primary Purpose

Donor Nephrectomy

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Periumbilical incision
Pfannenstiel incision
Sponsored by
University Hospital Heidelberg
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Donor Nephrectomy focused on measuring Physical Activity, Pfannenstiel incision, Periumbilical incision

Eligibility Criteria

20 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age > 20 years
  • No permanent pain therapy
  • Kidneys with only a single artery and vein in the graft
  • Informed consent for participation provided

Exclusion Criteria:

  • Infection or scar present precluding incision placement at one of the randomization sites
  • Bleeding disorders
  • Chronic use of immunosuppressive agents (e.g. steroids)

Sites / Locations

  • Division of Visceral Transplantation, Department of General, Visceral and Transplantation Surgery, University of HeidelbergRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Periumbilical incisions

Pfannenstiel incision

Arm Description

Outcomes

Primary Outcome Measures

Days to return to normal physical activity
Patients will be asked to complete the "Katz basic activities of daily living" self-maintenance questionnaire each day for 4 weeks after the operation. This questionnaire assesses the ability to perform daily living activities (0 = no activity and 6 = normal activity). The normal physical activity is perceived as good.

Secondary Outcome Measures

Warm ischemia time
From the time of clamping of the first renal artery in situ to flushing of the kidney with chilled solution on the back table
Intraoperative complications
From skin incision to skin closure
Estimated blood loss
From skin incision to skin closure
Operating time
From skin incision to skin closure
Postoperative pain
Severity of pain via 11-point Visual Analogue Scale (0 = no pain and 10 = unbearable distress).
Rescue analgesic
Total amount of analgesics required.
Peak expiratory flow rate
Is defined as maximum speed of expiration, as measured with a peak flow meter.
Postoperative complications
According to the Clavien-Dindo classification
Length of hospital stay
From the day of the operation until the day of discharge
Time to return to work
From the day of discharge and return to work
Physical activity score
The International Physical Activity Questionnaire, Short Form (IPAQ) will be used as an indicator of physical activity and fitness. IPAQ assesses total physical activity in the previous 7 days. Questions measure the frequency (days per week) and duration (minutes per session) of physical activity, as well as its intensity level (vigorous, moderate, walking, or sitting). Participants are categorized into one of three physical activity levels (low, moderate, high). Range is not applicable because it is a categorical variable. The high activity category is perceived as good.
Patient satisfaction
Patient satisfaction score via 5-point Likert scale (5 = representing strongly satisfied and 1 = representing strongly unsatisfied).
Cosmetic score
As defined by the Stony Brook scar scale (SBSES). The SBSES assessed five scar components: width, height, color, suture marks and overall appearance. Each component was assigned a score of 0 or 1 with a total sum range of 0 (worst) to 5 (best).
Incisional hernia
Defined as a fascia or muscle defect (bulging hernial sac and palpable fascia gap) at the site of the surgical incision examined by palpation and ultrasonography.
Mortality
Death due to any cause.
Recipient serum creatinine level
Serum creatinine level (mg/dL)
Glomerular filtration rate
GFR (mL/min/1.73 m2) calculated with "175 × (Scr)-1.154 × (Age)-0.203 × (0.742 if female)" Formula
Delayed graft function
Is defined as the need for one or more hemodialysis treatments following transplantation prior to the onset of graft function.
Primary non-function
A recipient whose graft never functions.

Full Information

First Posted
October 6, 2017
Last Updated
May 8, 2018
Sponsor
University Hospital Heidelberg
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1. Study Identification

Unique Protocol Identification Number
NCT03317184
Brief Title
Hand-assisted Laparoscopic Donor Nephrectomy Periumbilical Versus Pfannenstiel Incision
Acronym
HAPERPACT
Official Title
Hand-Assisted Laparoscopic Donor Nephrectomy PERiumbilical Versus Pfannenstiel Incision and Return to Normal Physical ACTivity: A Randomized Clinical Trial: HAPERPACT Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2017 (Actual)
Primary Completion Date
February 1, 2020 (Anticipated)
Study Completion Date
June 1, 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital Heidelberg

4. Oversight

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

5. Study Description

Brief Summary
Despite efforts to optimize the transplantation of deceased donor kidneys, the number of available kidneys continues to fall short of the demand. Living donor kidneys have been used to overcome this shortage. Graft and patient survival is significantly higher following living donor kidney transplantation compared with deceased donor kidney transplantation. Open donor nephrectomy was the universal technique prior to the advent of laparoscopic techniques. Laparoscopic approaches have definite advantages over open surgery in terms of blood loss, postoperative pain, analgesic requirements, duration of hospital stay, and convalescence. There is some controversy regarding longer warm ischemia time, longer operative time, and increased bleeding with laparoscopic nephrectomy compared with hand-assisted laparoscopic living donor nephrectomy (HALDN). HALDN attempted to reduce warm ischemia time by using the hand port to extract the kidney instantly after dividing the blood vessels. This technique also offers tactile feedback, better manual control of bleeding, a relatively shorter learning curve, less kidney traction, faster kidney removal, and shorter warm ischemic periods. HALDN is often performed using periumbilical and Pfannenstiel incisions for hand-assisted port placement. Pfannenstiel incisions improve wound complications such as incisional hernia, cosmetic issues, and wound dehiscence. However, duration of surgery, postoperative pain score, and length of hospital stay are significantly lower in donors with periumbilical incisions.To the best of our knowledge, these two types of incision have not been compared in a randomized controlled trial in patients undergoing HALDN. Our objective is to compare the results of Pfannenstiel incision (intervention group) with periumbilical incision (control group). The return to normal physical activity will be evaluated in a clinical randomized trial using an expertise-based design.
Detailed Description
Despite all efforts to optimize the transplantation of deceased donor kidneys, the number of available kidneys continues to fall short of demand. Living donor kidneys have been used to overcome this organ shortage. Graft and patient survival is significantly higher following living donor kidney transplantation compared with deceased donor kidney Transplantation. The major disadvantage of using living donors is that a healthy individual must undergo a major surgical procedure to provide the organ for transplantation. The donor does not medically benefit from the procedure, but there is a medical impact on both donor and recipient. Therefore, a nephrectomy technique associated with the lowest donor risk and the best organ quality should be used during Transplantation. Open donor nephrectomy was the universal technique before the advent of laparoscopic techniques. Laparoscopic living donor nephrectomy was introduced in 1995 and commercial ports were developed shortly after. In 1998, Wolf et al. described the hand-assisted laparoscopic living donor nephrectomy (HALDN) technique and since then it has become widely adopted. Laparoscopic methods have definite advantages over open surgery in terms of blood loss, postoperative pain, analgesic requirements, duration of hospital stay, and convalescence. There is some controversy regarding the possibility of relatively longer warm ischemia time, longer operative time, and increased bleeding with laparoscopic nephrectomy. HALDN reduces warm ischemia time by extracting the kidney using the hand port as soon as the blood vessels are divided. This technique is associated with tactile feedback, better manual control of bleeding, relatively shorter learning curve, less kidney traction, faster kidney removal, and shorter warm ischemic periods. At present, there is no strong evidence to support the use of one laparoscopic approach in preference to the other. However, evidence suggests that HALDN is the most cost-effective method of donor surgery and achieves equivalent clinical benefits of pure laparoscopic approaches with less operative time. HALDN is usually performed using a periumbilical or Pfannenstiel incision for hand-assisted port placement and kidney extraction. A periumbilical incision is made at the midline. In contrast, a Pfannenstiel incision is made as a slightly curved horizontal line just above the pubic symphysis. Pfannenstiel incisions improve wound complications, such as incisional hernia, cosmetic results, and wound dehiscence. However, the duration of surgery, postoperative pain score, and length of hospital stay were significantly lower in donors with periumbilical incision. The inserted hand plays a vital role in the procedure, including retraction and dissection, therefore the hand port midline incision is placed close to the periumbilical area. Dissecting the upper pole of the kidney through a Pfannenstiel incision may be difficult in morbidly obese and large donors. Patients with Pfannenstiel incisions return to normal physical activity quicker than those with periumbilical incisions. However, to the best of our knowledge, these two different incision types in patients undergoing HALDN have not been compared in a randomized controlled trial.Our objective is to compare the return of patients to physical activity following a HALDN procedure with Pfannenstiel incision (intervention group) or periumbilical incision (control group) in a clinical randomized trial using an expertise-based design.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Donor Nephrectomy
Keywords
Physical Activity, Pfannenstiel incision, Periumbilical incision

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Expertise-based, single intuition, assessor-blinded, randomized clinical trial.
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
52 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Periumbilical incisions
Arm Type
Experimental
Arm Title
Pfannenstiel incision
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Periumbilical incision
Intervention Description
A periumbilical incision is made at the abdominal midline for hand-assisted laparoscopic donor nephrectomy.
Intervention Type
Procedure
Intervention Name(s)
Pfannenstiel incision
Intervention Description
Pfannenstiel incision is made as a slightly curved horizontal line just above the pubic symphysis for hand-assisted laparoscopic donor nephrectomy.
Primary Outcome Measure Information:
Title
Days to return to normal physical activity
Description
Patients will be asked to complete the "Katz basic activities of daily living" self-maintenance questionnaire each day for 4 weeks after the operation. This questionnaire assesses the ability to perform daily living activities (0 = no activity and 6 = normal activity). The normal physical activity is perceived as good.
Time Frame
Four weeks
Secondary Outcome Measure Information:
Title
Warm ischemia time
Description
From the time of clamping of the first renal artery in situ to flushing of the kidney with chilled solution on the back table
Time Frame
One day
Title
Intraoperative complications
Description
From skin incision to skin closure
Time Frame
One day
Title
Estimated blood loss
Description
From skin incision to skin closure
Time Frame
One day
Title
Operating time
Description
From skin incision to skin closure
Time Frame
One day
Title
Postoperative pain
Description
Severity of pain via 11-point Visual Analogue Scale (0 = no pain and 10 = unbearable distress).
Time Frame
Seven days
Title
Rescue analgesic
Description
Total amount of analgesics required.
Time Frame
Seven days
Title
Peak expiratory flow rate
Description
Is defined as maximum speed of expiration, as measured with a peak flow meter.
Time Frame
Seven days
Title
Postoperative complications
Description
According to the Clavien-Dindo classification
Time Frame
60 days
Title
Length of hospital stay
Description
From the day of the operation until the day of discharge
Time Frame
60 days
Title
Time to return to work
Description
From the day of discharge and return to work
Time Frame
60 days
Title
Physical activity score
Description
The International Physical Activity Questionnaire, Short Form (IPAQ) will be used as an indicator of physical activity and fitness. IPAQ assesses total physical activity in the previous 7 days. Questions measure the frequency (days per week) and duration (minutes per session) of physical activity, as well as its intensity level (vigorous, moderate, walking, or sitting). Participants are categorized into one of three physical activity levels (low, moderate, high). Range is not applicable because it is a categorical variable. The high activity category is perceived as good.
Time Frame
60 days
Title
Patient satisfaction
Description
Patient satisfaction score via 5-point Likert scale (5 = representing strongly satisfied and 1 = representing strongly unsatisfied).
Time Frame
60 days
Title
Cosmetic score
Description
As defined by the Stony Brook scar scale (SBSES). The SBSES assessed five scar components: width, height, color, suture marks and overall appearance. Each component was assigned a score of 0 or 1 with a total sum range of 0 (worst) to 5 (best).
Time Frame
60 days
Title
Incisional hernia
Description
Defined as a fascia or muscle defect (bulging hernial sac and palpable fascia gap) at the site of the surgical incision examined by palpation and ultrasonography.
Time Frame
60 days
Title
Mortality
Description
Death due to any cause.
Time Frame
60 days
Title
Recipient serum creatinine level
Description
Serum creatinine level (mg/dL)
Time Frame
30 days
Title
Glomerular filtration rate
Description
GFR (mL/min/1.73 m2) calculated with "175 × (Scr)-1.154 × (Age)-0.203 × (0.742 if female)" Formula
Time Frame
30 days
Title
Delayed graft function
Description
Is defined as the need for one or more hemodialysis treatments following transplantation prior to the onset of graft function.
Time Frame
30 days
Title
Primary non-function
Description
A recipient whose graft never functions.
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age > 20 years No permanent pain therapy Kidneys with only a single artery and vein in the graft Informed consent for participation provided Exclusion Criteria: Infection or scar present precluding incision placement at one of the randomization sites Bleeding disorders Chronic use of immunosuppressive agents (e.g. steroids)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yakup Kulu, MD
Phone
0049 - 6221 - 5637215
Email
Yakup.Kulu@med.uni-heidelberg.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yakup Kulu, MD
Organizational Affiliation
Department of General, Visceral and Transplant Surgery, University Hospital Heidelberg, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Arianeb Mehrabi, MD
Organizational Affiliation
Department of General, Visceral and Transplant Surgery, University Hospital Heidelberg, Germany
Official's Role
Study Director
Facility Information:
Facility Name
Division of Visceral Transplantation, Department of General, Visceral and Transplantation Surgery, University of Heidelberg
City
Heidelberg
State/Province
Baden-Württemberg
ZIP/Postal Code
69120
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arianeb Mehrabi, MD
Phone
0049 - 6221 - 5636223
Email
arianeb.mehrabi@med.uni-heidelberg.de

12. IPD Sharing Statement

Citations:
PubMed Identifier
30005640
Citation
Kulu Y, Muller-Stich BP, Ghamarnejad O, Khajeh E, Polychronidis G, Golriz M, Nickel F, Benner L, Knebel P, Diener M, Morath C, Zeier M, Buchler MW, Mehrabi A. Hand-Assisted laparoscopic donor nephrectomy PERiumbilical versus Pfannenstiel incision and return to normal physical ACTivity (HAPERPACT): study protocol for a randomized controlled trial. Trials. 2018 Jul 13;19(1):377. doi: 10.1186/s13063-018-2775-4.
Results Reference
derived

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Hand-assisted Laparoscopic Donor Nephrectomy Periumbilical Versus Pfannenstiel Incision

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