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Single Site Versus Multi Site Robotic Hysterectomy

Primary Purpose

Rehabilitation, Pain, Postoperative, Wound Infection

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Robotic assisted hysterectomy
Sponsored by
Herning Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rehabilitation focused on measuring Return-to-work, Cosmesis, Visual analogue pain score

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Hysterectomy on benign indication,
  • American Society of Anesthetists group 1 or 2,
  • BMI less than 30 kg/m2
  • uterine size less than 300 g estimated by ultrasound, using Ferraris formula.

Exclusion Criteria:

  • adhesions
  • prior extensive abdominal surgery
  • prior midline incision
  • cutis laxa of abdomen surgery
  • endometriosis
  • more than 1 cesarean section
  • malignant disease

Sites / Locations

  • Gynecology Dept. Herning Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Robotic single-site hysterectomy

Robotic multi-site hysterectomy

Arm Description

Robotic single-site hysterectomy is performed in this arm

Robotic multi-site hysterectomy is performed in this arm

Outcomes

Primary Outcome Measures

Scar appearance and satisfaction
Appearance and evaluation of scar by POSAS scale (see www.posas.org and reference below) which has a scale from 1-10, where 1 is minimum and 10 is maximum; on scar's pain, its itching, on difference from normal skin, on stiffness, on thickness, on irregularity and general satisfaction

Secondary Outcome Measures

Scoring of abdominal pain
Visual analogue pain score with a minimum '0' and maximum '10'

Full Information

First Posted
June 7, 2018
Last Updated
September 6, 2018
Sponsor
Herning Hospital
Collaborators
Herlev Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03662451
Brief Title
Single Site Versus Multi Site Robotic Hysterectomy
Official Title
Single Site Versus Multi Site Robotic Hysterectomy
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2018 (Anticipated)
Primary Completion Date
November 1, 2021 (Anticipated)
Study Completion Date
November 1, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Herning Hospital
Collaborators
Herlev Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Robotic single site surgery (R-SSH) is a novel technique, which may be superior to multi site hysterectomy (R-MSH) in select patients regarding cosmesis and postoperative pain. A randomized trial is performed to compare R-SSH with R-MSH with regard to the postoperative rehabilitation, cosmesis, the operational cost, and the perioperative morbidity.
Detailed Description
The study is scheduled to start November 2018 and compares robotic single site to multi site hysterectomy. Procedures are performed on two locations, Herning and Herlev Hospitals, by experienced surgeons. Patients are randomized to either R-SSH (No.=62) or R-MSH (No.=62). Patient's satisfaction with body image and cosmesis is assessed at different time points pre- and postoperatively by means of validated cosmesis scales and Body Image Questionnaire and photo-evaluations. Postoperative pain and split times spent at the operation theatre will be registered as secondary outcome parameters. A follow-up at 1, 3 and 6 month include evaluation of the scar and registration of port-site hernias and vaginal dehiscence or other complications. Interviews and diaries will include time of return to home and work, daily activities including sexuality The R-SSH is performed using da Vinci, Xi robotic system. One single port, diameter 2 cm is applied. Applying an additional assistant port is defined conversion of procedure R-MSH is performed using standard equipment and 4 trocars, 5 mm each. Sample size calculation was based a previous study on fast track hysterectomy, which showed a difference in return to work of 4 days. 62 women in each group is needed with standard deviation ±8 and a power of 80%. To include those not working, the calculation was performed with an expected visual analog pain score of 0.86 ±0.2 and 62 in each group and suggested that the sample was sufficient to detect of difference of 0.1 in visual analog pain score with a power of 80%. All calculation are based on two-sided testing with alpha of 0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rehabilitation, Pain, Postoperative, Wound Infection
Keywords
Return-to-work, Cosmesis, Visual analogue pain score

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Women are randomized to either robotic single site or multi site hysterectomy
Masking
None (Open Label)
Allocation
Randomized
Enrollment
124 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robotic single-site hysterectomy
Arm Type
Active Comparator
Arm Description
Robotic single-site hysterectomy is performed in this arm
Arm Title
Robotic multi-site hysterectomy
Arm Type
Active Comparator
Arm Description
Robotic multi-site hysterectomy is performed in this arm
Intervention Type
Procedure
Intervention Name(s)
Robotic assisted hysterectomy
Intervention Description
Periumbilical single incision vs multiple abdominal incisions for hysterectomy
Primary Outcome Measure Information:
Title
Scar appearance and satisfaction
Description
Appearance and evaluation of scar by POSAS scale (see www.posas.org and reference below) which has a scale from 1-10, where 1 is minimum and 10 is maximum; on scar's pain, its itching, on difference from normal skin, on stiffness, on thickness, on irregularity and general satisfaction
Time Frame
Six months after operation
Secondary Outcome Measure Information:
Title
Scoring of abdominal pain
Description
Visual analogue pain score with a minimum '0' and maximum '10'
Time Frame
Visual analogue pain score at first, second, third, fourth, fifth, and sixth month after operation

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hysterectomy on benign indication, American Society of Anesthetists group 1 or 2, BMI less than 30 kg/m2 uterine size less than 300 g estimated by ultrasound, using Ferraris formula. Exclusion Criteria: adhesions prior extensive abdominal surgery prior midline incision cutis laxa of abdomen surgery endometriosis more than 1 cesarean section malignant disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Finn F Lauszus, PhD
Phone
+45 78 434614
Email
finlau@rm.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Carsten Byrialsen
Phone
+45 21609156
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Finn F Lauszus, PhD
Organizational Affiliation
Herning Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Gynecology Dept. Herning Hospital
City
Herning
ZIP/Postal Code
7400
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Awaiting consensus in the steering Group on meeting, posters, abstracts, and publications
Citations:
PubMed Identifier
26992935
Citation
El Hachem L, Andikyan V, Mathews S, Friedman K, Poeran J, Shieh K, Geoghegan M, Gretz HF 3rd. Robotic Single-Site and Conventional Laparoscopic Surgery in Gynecology: Clinical Outcomes and Cost Analysis of a Matched Case-Control Study. J Minim Invasive Gynecol. 2016 Jul-Aug;23(5):760-8. doi: 10.1016/j.jmig.2016.03.005. Epub 2016 Mar 15.
Results Reference
background
PubMed Identifier
23140831
Citation
Golkar FC, Ross SB, Sperry S, Vice M, Luberice K, Donn N, Morton C, Hernandez JM, Rosemurgy AS. Patients' perceptions of laparoendoscopic single-site surgery: the cosmetic effect. Am J Surg. 2012 Nov;204(5):751-61. doi: 10.1016/j.amjsurg.2011.07.026.
Results Reference
background
PubMed Identifier
28357561
Citation
Sandberg EM, la Chapelle CF, van den Tweel MM, Schoones JW, Jansen FW. Laparoendoscopic single-site surgery versus conventional laparoscopy for hysterectomy: a systematic review and meta-analysis. Arch Gynecol Obstet. 2017 May;295(5):1089-1103. doi: 10.1007/s00404-017-4323-y. Epub 2017 Mar 29.
Results Reference
background
PubMed Identifier
23312246
Citation
Yeung PP Jr, Bolden CR, Westreich D, Sobolewski C. Patient preferences of cosmesis for abdominal incisions in gynecologic surgery. J Minim Invasive Gynecol. 2013 Jan-Feb;20(1):79-84. doi: 10.1016/j.jmig.2012.09.008.
Results Reference
background
PubMed Identifier
26264829
Citation
Aarts JW, Nieboer TE, Johnson N, Tavender E, Garry R, Mol BW, Kluivers KB. Surgical approach to hysterectomy for benign gynaecological disease. Cochrane Database Syst Rev. 2015 Aug 12;2015(8):CD003677. doi: 10.1002/14651858.CD003677.pub5.
Results Reference
background
PubMed Identifier
20596233
Citation
Fearmonti R, Bond J, Erdmann D, Levinson H. A review of scar scales and scar measuring devices. Eplasty. 2010 Jun 21;10:e43.
Results Reference
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Single Site Versus Multi Site Robotic Hysterectomy

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