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OpenTrials
Completed

NCT Number: NCT01174069

Natural Orifice Transgastric Endoscopic Surgical Removal of the Gallbladder

Hypothesis: Natural orifice transgastric cholecystectomy with laparoscopic assist will be feasible and have comparable complication rates as standard lap cholecystectomy. Patient benefits will include less pain and scaring.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Legacy health System

Portland, Oregon, 97210, United States

About this study

In this study, we propose to use a surgical technique that eliminates the need for a 1.5-2.5 cm umbilical incision. A flexible endoscope will be inserted through the mouth and into the stomach. Using commercially available endoscopes, endoscopic instruments and accessories, a small incision will be made in the gastric wall and the endoscope will be advanced into the insufflated peritoneal cavity. Two to three small laparoscopic trocars will be placed for laparoscopic instrument insertion to manipulate, retract and cut tissue. The flexible endoscope will provide visualization of the surgical field and flexible endoscopic instruments may be used to augment surgical manipulation with the laparoscopic instruments. Once dissected free, the gall bladder will be removed through the stomach and out of the mouth. Commercially available endoscopic clips, sutures and/or tissue anchors will be used to close the gastrotomy; additionally, the gastrotomy will be tested for leaks and laparoscopically oversewn with suture as needed.

Patients will be discharged per the standard of practice for a laparoscopic cholecystectomy. During the hospital stay severity of pain and use of pain medications will be recorded. Length of time spent in the recovery room and in the hospital will also be collected. Patients will return and be evaluated by their surgeon two weeks following their procedure. At this visit, any complications will be noted in the patient's medical record. Additionally at this visit and at the preoperative visit, patients will complete a standardized Quality of Life (QOL) assessment (i.e., SF-36) and perceived pain levels and type and frequency of pain medications will be recorded in the patient's medical record.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ability to undergo general anesthesia
  • Age > 18 years of age and < 80 years of age
  • Ability to give informed consent

Exclusion criteria

  • Acute cholecystitis
  • Body Mass Index (BMI) > 40
  • Contraindicated for esophagogastroduodenoscopy (EGD)
  • Gallstones > 2.5cm in diameter
  • Gall bladder more than 15cm in length on U/S
  • Presence of common duct stones
  • Presence of esophageal stricture
  • Altered gastric anatomy

Treatment and study plan

NOTES assisted laparoscopic cholecystectomy

Procedure

Surgical removal of the gallbladder using endoscopic instruments.

Other names: NOTES Cholecystectomy

Primary outcomes

  1. Postoperative pain

    Time frame: 30 days

    perceived pain levels and type and frequency of pain medications will be recorded in the patient's medical record.

Secondary outcomes

  1. Perception of surgical outcome

    Time frame: 30 days post operatively

    standardized Quality of Life (QOL) assessment (i.e., SF-36) form filled out by the patient.

Sponsors and collaborators

Lead sponsor

The Oregon Clinic

Other

Collaborators

  • Northwestern University

Registry information

Official study title

Clinical Outcomes Trial of Laparoscopic Assisted Transgastric Endoscopic Cholecystectomy

Acronym: NOTESchole

Important dates

Study start
2007
Primary completion
2015
Study completion
2015
First posted
Aug 3, 2010
Registry last updated
Sep 3, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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