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This study is designed to be a United States multicenter prospective randomized controlled non-inferiority evaluation of transgastric and transvaginal Natural Orifice Translumenal Endoscopic Surgery (NOTES) cholecystectomy compared to laparoscopic cholecystectomy in elective surgery patients. Up to 200 patients will be enrolled to obtain 70 NOTES cholecystectomies (35 transgastric and 35 transvaginal) and 70 laparoscopic cholecystectomies on a randomized basis. In order to evaluate the hypothesis that NOTES cholecystectomy has equivalent safety and efficacy to laparoscopic cholecystectomy, clinical and administrative outcomes will be measured.
Full description
Primary To assess the safety and efficacy of transgastric and transvaginal cholecystectomy compared to conventional laparoscopic cholecystectomy.
To assess pain associated with transgastric and transvaginal cholecystectomy compared to conventional laparoscopic cholecystectomy.
Secondary To assess cosmesis associated with transgastric and transvaginal cholecystectomy compared to conventional laparoscopic cholecystectomy.
To assess objective operative cost and logistical comparisons between transgastric and transvaginal cholecystectomy compared to conventional laparoscopic cholecystectomy.
To identify unforeseen barriers to transgastric or transvaginal surgery adoption.
Enrollment
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Inclusion criteria
Competent male or female subjects, between the ages of 18-75 and who present for elective cholecystectomy will be offered participation in this study.
Male subjects must be willing to have the cholecystectomy by either the laparoscopic or transgastric NOTES approach.
Female subjects must be willing to have the cholecystectomy by either the laparoscopic or either the NOTES approaches (transgastric and/or transvaginal) being performed at the site.
Patients offered participation in this study must provide written, informed consent and meet the following criteria prior to randomization.
Diagnosis of benign gallstone disease which requires cholecystectomy.
ASA Class 1 or 2.
Willingness to have laparoscopic cholecystectomy performed and have research data collected for control group.
Willingness to have abdomen photographed (for cosmesis assessment).
For sites performing transgastric NOTES approach
For sites performing transvaginal NOTES approach - Female subjects only
Exclusion criteria
Pregnant women.
Obese patients (BMI > 35).
Patients with severe medical comorbidities (ie, NOT ASA Class 1 or 2) will be excluded such as:
Chronic renal failure
Chronic liver disease
Congestive heart failure
Patients with a presumed gallbladder malignancy.
Patients with a history of prior open abdominal or laparoscopic or transvaginal surgery. However patients with prior appendectomy, tubal ligation or Cesarean section will be included.
Patients who are taking immunosuppressive medications and/or immunocompromised.
Patients with a prior history of perineal trauma leading to significant alteration of vaginal anatomy.
Patients with a history of ectopic pregnancy, pelvic inflammatory disease, large fibroids or severe endometriosis.
Patients with known common bile duct stones. (ie, not cleared prior to surgery). Patients with common bile duct stones discovered intra-operatively will remain in the study.
Patients on anticoagulation drugs other than once daily aspirin. Abnormal blood coagulation tests. Minimal abnormalities may be allowed at the discretion of site principal investigator.
Gallstones> 2.5cm in diameter.
Presence of untreated esophageal stricture.
Surgically altered gastric anatomy or severe uncorrected paraesophageal types 2, 3 or 4.
Unwillingness to consent to NOTES procedure(s).
Acute cholecystitis or cholangitis
For sites performing transgastric NOTES approach
Primary purpose
Allocation
Interventional model
Masking
200 participants in 2 patient groups
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Central trial contact
Michael Kochman, MD; Steven L Schwaitzberg, MD
Data sourced from clinicaltrials.gov
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