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Feasibility of Transvaginal Cholecystectomy (TVC)

Primary Purpose

Gallstones

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Transvaginal Cholecystectomy
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gallstones focused on measuring Gallbladder removal

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion criteria

  • Female patients undergoing elective cholecystectomy for cholelithiasis.

Exclusion criteria

  • Male patients, patients <18 years or >65 years of age
  • Pregnant patients
  • Patients with prior pelvic surgery
  • Patients with prior hepatobiliary surgery or other major abdominal surgery
  • Patients with ASA class >3
  • Patients with BMI >35
  • Patients with risk factors for requiring an open cholecystectomy (e.g. possible gallbladder cancer, acute cholecystitis, jaundice)
  • Patients who cannot provide consent for the study
  • Patients not willing to participate in the study.
  • Patients with common bile duct stones
  • Patients with evidence of abdominal abscess or mass
  • Patients with diffuse peritonitis
  • Patients with a clinical diagnosis of sepsis
  • Patients with coagulopathy or using anticoagulants or anti-platelet agents (aspirin up to 81mg/day acceptable)
  • Patients with planned concurrent procedures
  • Patients with a prior diagnosis of intra-abdominal adhesions
  • Patients who are participating in any other investigational device or drug trial that has not yet completed the primary endpoint
  • Patients with an enlarged uterus

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Transvaginal Surgery

    Arm Description

    Gallbladder will be removed through the vagina

    Outcomes

    Primary Outcome Measures

    Feasibility measured by successful transvaginal removal of gallbladder
    The procedure will be considered technically successful if at completion the cystic duct and artery have been clipped securely and the gallbladder has been removed through the transvaginal port. At the time of surgery, the procedure will be supervised with a laparoscope at all critical points. Conversion to a laparoscopic or open procedure is considered an incomplete transvaginal procedure.

    Secondary Outcome Measures

    Safety and tolerability measured by individual and overall Adverse Events
    Procedural complications recorded during transvaginal cholecystectomy. Complications resulting from endoscopic transvaginal cholecystectomy recorded at the time of surgery. Patients' post-operative clinical course for duration of three months, including routine follow up at about one week after the operation, vaginal exam after six weeks and follow-up with quality of life questionnaire at three months.
    Pain Scores as measured on the Visual Analog Scale
    One of the main endpoints of the study will be postoperative pain as measured by the visual analog scale. The scale will be measured in triplicate fashion. In addition to the visual analog scale, the amount and class of pain medication used will be collected.
    Quality of Life measured through validated questionnaires
    Data for the SF-12 and ASIS will be scaled and evaluated for correlation at baseline and postoperative day 7 with the Pearson coefficient. Change from baseline for each instrument will be evaluated.

    Full Information

    First Posted
    October 28, 2010
    Last Updated
    January 12, 2016
    Sponsor
    Mayo Clinic
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01232959
    Brief Title
    Feasibility of Transvaginal Cholecystectomy
    Acronym
    TVC
    Official Title
    Feasibility of Transvaginal Cholecystectomy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2016
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Subjects not interested
    Study Start Date
    October 2010 (undefined)
    Primary Completion Date
    December 2012 (Actual)
    Study Completion Date
    December 2012 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Mayo Clinic

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Today there are three different ways to remove a gallbladder with gallstones. Surgeons can remove the gallbladder through small incisions in the abdomen. This is called laparoscopic cholecystectomy. It is the current standard. It has replaced traditional open gallbladder surgery. Open gallbladder surgery is done with a large incision. A new way of removing the gallbladder in women is through the vagina. This is called transvaginal cholecystectomy. This study is being done to see if removing the gallbladder through the vagina will work for patients at Mayo Clinic Rochester. This is the first step of this research to test the procedure. In the future, other studies will examine the potential for less scarring and reduced pain. In this study the investigators will still make small incisions in the abdomen, they will be smaller than the standard procedure but you will still have some scars on your abdomen. Some very early research reports say that some patients may have less pain with the transvaginal approach; however, the investigators do not know if the transvaginal route will have any effect on your overall health and quality of life. This study will evaluate: Effectiveness of the surgery: ability to remove the gallbladder safely Effect of the operation on your body: change in pulse and blood pressure during the surgery, level of inflammation markers in your blood before and after the surgery Recovery from surgery in the hospital: how much pain you have, how much pain medication you need, how long you need to stay in the hospital, or nature of any surgical complications (problems) Overall recovery from surgery: general quality of life, abdominal symptoms What is the new type of surgery? The new type of surgery is called transvaginal cholecystectomy: A small incision is made in the vagina. An endoscope (flexible lighted camera tube) is inserted into the abdomen. An endoscope is normally used to examine your stomach or colon. A very small camera is placed in your abdomen at the belly button (5 mm, ¼ inch). This helps the surgeons to remove your gallbladder through the vagina. The procedure to separate your gallbladder from your body will be assisted by instruments placed through your abdomen and instruments placed in your vagina. The surgeon will remove the gallbladder by passing it though your vagina.
    Detailed Description
    As technologic innovations in medicine continue to advance, less intrusive operative procedures are being developed. Natural Orifice Transluminal Endoscopic Surgery (NOTES) may represent a less invasive approach to the abdominal cavity. The access to the abdominal cavity through natural orifices such as the vagina has the benefit of decreased somato-sensory innervation. This venue might confer less pain and operative stress to the patient. The transvaginal approach has been suggested as a new surgical approach to gallbladder surgery (cholecystectomy). Approximately 700 transvaginal cholecystectomy procedures have been performed in medical centers around the world so far. Anecdotal data suggest that the patients experience less pain postoperatively and half of them may not require any pain medication. Currently, introduction of this new operative approach outside of a research study is not supported by national nor international societies. We wish to demonstrate that the transvaginal approach is feasible for 10 patients with gallstone disease at Mayo Clinic Rochester (MCR). Methods: Female patients seen by consultants from the Division of General and Gastrointestinal Surgery, who have an appropriate indication for elective cholecystectomy, will be offered a cholecystectomy via the transvaginal approach. After patient enrollment, baseline demographics, questionnaires and blood draws will be obtained. The patient will undergo a laparoscopic assisted transvaginal cholecystectomy by a dedicated surgical team, consisting of a gynecologist, a minimally invasive surgeon and a gastroenterologist. This approach will utilize a 5-mm umbilical trocar and a posterior colpotomy. Standard laparoscopic and flexible endoscopic instrumentation will be utilized along with recently introduced long flexible-tip laparoscopic instrumentation to remove the gallbladder. Intraoperative parameters will be recorded. Postoperatively blood draws and questionnaires will be repeated at specific intervals. Data analysis will be mainly descriptive for this feasibility study. The collected material will serve as pilot data for a future comparative study of transvaginal cholecystectomy with standard laparoscopic cholecystectomy.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Gallstones
    Keywords
    Gallbladder removal

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Transvaginal Surgery
    Arm Type
    Experimental
    Arm Description
    Gallbladder will be removed through the vagina
    Intervention Type
    Device
    Intervention Name(s)
    Transvaginal Cholecystectomy
    Other Intervention Name(s)
    gallbladder removal
    Intervention Description
    A small incision is made in the vagina. An endoscope (flexible lighted camera tube) is inserted into the abdomen. An endoscope is normally used to examine your stomach or colon. A very small camera is placed in your abdomen at the belly button (5 mm, ¼ inch). This helps the surgeons to remove your gallbladder through the vagina. The procedure to separate your gallbladder from your body will be assisted by instruments placed through your abdomen and instruments placed in your vagina. The surgeon will remove the gallbladder by passing it though your vagina.
    Primary Outcome Measure Information:
    Title
    Feasibility measured by successful transvaginal removal of gallbladder
    Description
    The procedure will be considered technically successful if at completion the cystic duct and artery have been clipped securely and the gallbladder has been removed through the transvaginal port. At the time of surgery, the procedure will be supervised with a laparoscope at all critical points. Conversion to a laparoscopic or open procedure is considered an incomplete transvaginal procedure.
    Time Frame
    1 year
    Secondary Outcome Measure Information:
    Title
    Safety and tolerability measured by individual and overall Adverse Events
    Description
    Procedural complications recorded during transvaginal cholecystectomy. Complications resulting from endoscopic transvaginal cholecystectomy recorded at the time of surgery. Patients' post-operative clinical course for duration of three months, including routine follow up at about one week after the operation, vaginal exam after six weeks and follow-up with quality of life questionnaire at three months.
    Time Frame
    Following each surgery but overall at 1 year
    Title
    Pain Scores as measured on the Visual Analog Scale
    Description
    One of the main endpoints of the study will be postoperative pain as measured by the visual analog scale. The scale will be measured in triplicate fashion. In addition to the visual analog scale, the amount and class of pain medication used will be collected.
    Time Frame
    1 year
    Title
    Quality of Life measured through validated questionnaires
    Description
    Data for the SF-12 and ASIS will be scaled and evaluated for correlation at baseline and postoperative day 7 with the Pearson coefficient. Change from baseline for each instrument will be evaluated.
    Time Frame
    1 year

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    65 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion criteria Female patients undergoing elective cholecystectomy for cholelithiasis. Exclusion criteria Male patients, patients <18 years or >65 years of age Pregnant patients Patients with prior pelvic surgery Patients with prior hepatobiliary surgery or other major abdominal surgery Patients with ASA class >3 Patients with BMI >35 Patients with risk factors for requiring an open cholecystectomy (e.g. possible gallbladder cancer, acute cholecystitis, jaundice) Patients who cannot provide consent for the study Patients not willing to participate in the study. Patients with common bile duct stones Patients with evidence of abdominal abscess or mass Patients with diffuse peritonitis Patients with a clinical diagnosis of sepsis Patients with coagulopathy or using anticoagulants or anti-platelet agents (aspirin up to 81mg/day acceptable) Patients with planned concurrent procedures Patients with a prior diagnosis of intra-abdominal adhesions Patients who are participating in any other investigational device or drug trial that has not yet completed the primary endpoint Patients with an enlarged uterus
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Juliane Bingener-Casey, MD
    Organizational Affiliation
    Mayo Clinic
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Feasibility of Transvaginal Cholecystectomy

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