Minimally Invasive Benign Hysterectomy

Sponsor
Region Skane (Other)
Overall Status
Unknown status
CT.gov ID
NCT01865929
Collaborator
(none)
200
1
2
71
2.8

Study Details

Study Description

Brief Summary

A randomised controlled trial comparing hysterectomy by minimally invasive surgical methods; robotic hysterectomy versus vaginal hysterectomy or traditional laparoscopic hysterectomy; outcome and cost analyses.

Condition or Disease Intervention/Treatment Phase
  • Device: Robotic hysterectomy
  • Procedure: Vaginal or laparoscopic hysterectomy
N/A

Detailed Description

Laparoscopic surgery is advantageous compared to open surgery in terms of patient morbidity, shorter hospitalization and a more rapid return to daily activities. Robot-assisted laparoscopic surgery have facilitated a higher proportion of minimally invasive surgery first and foremost within gynecologic oncology.It is not clear whether or not this is true for less advanced surgery where a vaginal approach or a traditional laparoscopic approach is possible.

Robot-assisted surgery is associated with additional cost due to investment and more expensive surgical equipment. The study is performed to investigate whether or not performing hysterectomy for benign conditions with robotic surgery will be advantageous in terms of shorter operating time, less complications, less conversions to open surgery, and shorter hospital stay in comparison to other minimally invasive procedures such as vaginal hysterectomy and traditional laparoscopic hysterectomy.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Benign Hysterectomy; a Randomized Controlled Trial Comparing Robotic Hysterectomy With Vaginal Hysterectomy and Traditional Laparoscopic Hysterectomy
Study Start Date :
Jan 1, 2010
Anticipated Primary Completion Date :
Sep 1, 2014
Anticipated Study Completion Date :
Dec 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Robotic hysterectomy

Minimally invasive hysterectomy by robotic surgery

Procedure: Vaginal or laparoscopic hysterectomy
Benign hysterectomy performed by traditional minimal invasive procedures.

Active Comparator: Vaginal or laparoscopic hysterectomy

Minimal invasive hysterectomy by vaginal or traditional laparoscopic surgery.

Device: Robotic hysterectomy
Minimally invasive hysterectomy for benign disorders. Comparing robotic hysterectomy with vaginal hysterectomy and traditional laparoscopic hysterectomy
Other Names:
  • da Vinci Surgical system, Intuitive Surgical Inc, CA, USA
  • Outcome Measures

    Primary Outcome Measures

    1. Cost of surgery [4 months]

      The cost of surgery includes the actual surgery (anaesthesia, OR-nurse, circulating nurse, doctors and use of the OR) as well as the length of the inpatient stay. The cost for conversions to open surgery, reoperations, readmissions, and any additional cost associated with additional procedures or medical interventions such as radiological examinations and blood transfusions. Based on the estimated cost of surgical material, use of the operating room and cost of anaesthesia each benign hysterectomy performed with robotic surgery would need to be 50 minutes shorter than other minimal invasive procedures to compensate for the additional cost.

    Secondary Outcome Measures

    1. Patient outcome [4 months]

      The number of patients in whom an intraoperative or postoperative complication occurs as well as the seriousness of the complication which occurs and what this entails for the patient in question. This includes conversions to open surgery as well as the need for reoperation and readmission.

    Other Outcome Measures

    1. Social cost [4 months]

      The length of postoperative sick leave and reasons for extending sick leave and cost thereof.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    25 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • indication for hysterectomy for benign disease or prophylactic surgery due to hereditary cancer

    • size of uterus and vagina allows for retrieval by the vaginal route

    • maximum uterine size equivalent to 16 weeks of pregnancy

    • informed consent

    Exclusion Criteria:
    • malignant disease

    • known extensive intra-abdominal adhesions

    • anaesthesiological contraindications to laparoscopic surgery

    • women with pacemaker or other implants where electrosurgery is to be avoided

    • immunoincompetent women

    • simultaneous need for prolapse surgery

    • women with known defects of the hemostasis

    • allergies towards metronidazole and doxycycline

    • inability to understand patient information

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Department of Obstetrics and Gynecology, Skane University Hospital Lund Sweden 221 85

    Sponsors and Collaborators

    • Region Skane

    Investigators

    • Study Director: Jan Persson, MD, PhD, Department of Obstetrics and Gynecology, Skane University Hospital, Lund

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Celine Lönnerfors, Medical Doctor, Region Skane
    ClinicalTrials.gov Identifier:
    NCT01865929
    Other Study ID Numbers:
    • LundKK
    First Posted:
    May 31, 2013
    Last Update Posted:
    May 31, 2013
    Last Verified:
    May 1, 2013

    Study Results

    No Results Posted as of May 31, 2013