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Cholecystolithiasis clinical trials

View clinical trials related to Cholecystolithiasis.

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NCT ID: NCT00940264 Completed - Cholecystitis Clinical Trials

Laparoscopic Transvaginal Hybrid Cholecystectomy: a Prospective Data Collection.

Start date: September 2008
Phase: N/A
Study type: Observational

Transvaginal hybrid procedures especially the transvaginal hybrid cholecystectomy are of interest as an available NOTES-Procedure for the clinical routine. Few authors have demonstrated the feasibility and safety in a selected patient collective. The aim of this prospective data collection is to evaluate the feasibility in the clinical routine in a non select patient collective. Therefore all patients giving the informed consent to the transvaginal hybrid cholecystectomy will be included and assessed concerning feasibility to perform the transvaginal approach and complete the operation transvaginally.

NCT ID: NCT00910325 Terminated - Cholelithiasis Clinical Trials

Natural Orifice Translumenal Endoscopic Surgery: Laparoscopic-Assisted Transvaginal Cholecystectomy

Start date: November 2008
Phase: Phase 1/Phase 2
Study type: Interventional

To determine the feasibility, safety, and efficacy of a novel minimally invasive approach to cholecystectomy and to establish a description of this novel translumenal technique in humans at this institution.

NCT ID: NCT00904865 Recruiting - Cholecystitis Clinical Trials

Single Port Access (SPA) Cholecystectomy Versus Standard Laparoscopic Cholecystectomy

Start date: February 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Background: Single port access surgery is a rapidly progressing surgical approach which allows performance of standard laparoscopic surgery through a single transparietal port instead of multiple port accesses. Objective: Demonstrate the validity of Single port access (SPA) cholecystectomy compared to multiple ports laparoscopic cholecystectomy. Hypothesis: SPA cholecystectomy is associated with decreased parietal and body image trauma compare to multiple ports laparoscopic cholecystectomy. SPA cholecystectomy should be associated with better cosmetic results, may improve postoperative recovery due to lower parietal pain. SPA cholecystectomy may also be associated with decreased rate of parietal complications as lower numbers of transparietal port are placed. Methods: All patients offered cholecystectomy, either SPA or multiport cholecystectomy, included in the study will have recognized biliary pathology for which formal indication cholecystectomy are recognized internationally. Surgical technique, either for SPA cholecystectomy or for multiple ports cholecystectomy, will be the same except, that one surgical technique is achieved through a single transparietal port and the other through multiple ports. Randomization will be performed before surgeries after patients have given their informed consent to the study. No specific test or cost will be necessitated by the study. Patients will be informed orally and will receive a short study summary, allowing them to give an informed consent. Endpoints: - Morbidity - Body image and Cosmetic results - Post-operative pain (opioid sparing effect) - Operative time - Hospital stay

NCT ID: NCT00890201 Completed - Clinical trials for Pancreaticobiliary Reflux

Pancreaticobiliary Reflux in Patients Without Cholelithiasis

Start date: January 2009
Phase: N/A
Study type: Observational

Pancreaticobiliary reflux has been found in patients with cholelithiasis and gallbladder cancer associated with normal pancreaticobiliary union. However, the presence of pancreaticobiliary reflux has not been studied in patients without gallstones (healthy gallbladders). The authors believe that pancreaticobiliary reflux might be a normal phenomenon in patients with and without gallstones, although in patients with cholelithiasis it might constitute a pathological condition associated with dismotility of the biliary tree and the sphincter of Oddi.

NCT ID: NCT00863642 Completed - Clinical trials for Gallstone Pancreatitis

Early Versus Delayed Surgery for Gallstone Pancreatitis

Start date: November 2007
Phase: N/A
Study type: Interventional

While there exists consensus among surgeons that patients with gallstone pancreatitis should undergo cholecystectomy to prevent recurrence, the precise timing of laparoscopic cholecystectomy for mild to moderate disease remains controversial. We hypothesize that laparoscopic cholecystectomy performed within 48 hours of admission, regardless of resolution of abdominal pain or abnormal laboratory values, will result in a shorter hospital stay.

NCT ID: NCT00836316 Completed - Pain Clinical Trials

Levobupivacaine During Cholecystectomy

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effects of intraperitoneal administration of levobupivacaine on pain after laparoscopic cholecystectomy.

NCT ID: NCT00835250 Completed - Cholelithiasis Clinical Trials

Laparoscopic Cholecystectomy vs Hybrid Natural Orifice Translumenal Surgery

Start date: February 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to determine the feasibility of cholecystectomy made by a transvaginal approach with a NOTES procedure (natural orifice translumenal endoscopic surgery).

NCT ID: NCT00815438 Withdrawn - Cholecystitis Clinical Trials

Transvaginal Cholecystectomy Using Endoscopic Assistance

Start date: January 2009
Phase: Phase 1
Study type: Interventional

Surgical removal of the gallbladder is needed in 1 million people per year in the USA. The procedure is done by placing four tubes (cannula) from 5 to 10 mm through the abdominal wall. Air is placed in the abdominal cavity and a lighted scope is placed through one cannula. The space in the abdominal cavity can then be seen on a video screen. Thin retractors and dissecting instruments are placed through the other cannula and the gallbladder is removed using the video screen for vision. The gallbladder duct and the artery are usually occluded with clips or stitches. In this study we propose to do the procedure though a single 5 mm incision placed at the umbilicus and a second access through the vagina using a flexible endoscope. The gallbladder will be retracted using strings (sutures) attached to the gallbladder. The dissection will be done using laparoscopic instruments (scissors, knives, dissectors) placed through the laparoscopic port. A flexible grasper may be used in the endoscope to help with retraction. An endoscopic snare or grasper will be used to grasp the gallbladder and remove it from the abdomen through the vagina. This study evaluates the ability to do laparoscopic cholecystectomy with one skin incision and one vaginal incision. This will provide the basis for future studies evaluating decreased pain and costs with transvaginal assisted cholecystectomy.

NCT ID: NCT00792389 Not yet recruiting - Gallstone Clinical Trials

Study of the Use of Humidified Warmed Gas and the Effect on Post-Operative Pain in Laparoscopic Cholecystectomies

Start date: January 2009
Phase: Phase 4
Study type: Interventional

Double blind RCT comparing elective laparoscopic cholecystectomy using warmed, humidified gas (new) against laparoscopic cholecystectomy with cool, dry gas (usual). Sample size of 200 patients. Outcome measures are postoperative opiate analgesia use, and post operative numerical pain scores.

NCT ID: NCT00732550 Completed - Cholelithiasis Clinical Trials

Comparison of Single Trocar Cholecystectomy to Standard Laparoscopic Cholecystectomy

Start date: July 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the advantages of single trocar cholecystectomy over standard laparoscopic cholecystectomy.