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Cholecystectomy, Laparoscopic clinical trials

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NCT ID: NCT03258177 Completed - Clinical trials for Cholecystectomy, Laparoscopic

Virtual Visits (Utilization of Virtual Care in Postoperative Patients to Improve the Patient Experience)

Start date: August 18, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to implement and evaluate postoperative virtual care visits for patients who undergo a laparoscopic appendectomy, laparoscopic cholecystectomy, or robotic cholecystectomy. The investigators aim to better understand whether postoperative virtual care visits will not result in a greater composite measure of the occurrence of hospital encounters within Atrium Health (AH) for the 30 days following surgery than standard in-person clinic care. The investigators also aim to better understand whether postoperative virtual care visits provide time and cost savings, and provide equal or improved patient satisfaction and convenience.

NCT ID: NCT03241875 Completed - Pain, Postoperative Clinical Trials

Effects of Preoperative Gabapentin Versus Pregabalin on Shoulder Pain After Laparoscopic Cholecystectomy

Start date: December 1, 2016
Phase: Phase 4
Study type: Interventional

The aim of this study is to evaluate the effect of premedication with pregabalin or gabapentin versus placebo on postoperative shoulder pain after laparoscopic cholecystectomy.

NCT ID: NCT03155321 Terminated - Cholelithiasis Clinical Trials

SAGES Safe Cholecystectomy Program in Polish Reality - Awareness, Implementation and Opinion on Usefulness

Start date: April 1, 2017
Phase:
Study type: Observational

The study is designed to assess the awareness of the SAGES Safe Cholecystectomy Program among polish surgeons, as well as the degree of implementation of this Program during laparoscopic cholecystectomy performed in Poland. It also gathers the opinion of polish surgeons on usefulness of each of the SAGES Safe Cholecystectomy Rules

NCT ID: NCT03133494 Completed - Clinical trials for Cholecystectomy, Laparoscopic

Arterial Blood Gas Analysis in Laparoscopic Cholecystectomy

ABG
Start date: April 1, 2015
Phase: N/A
Study type: Interventional

The investigator found out that as such the base line carbon dioxide (CO2) level is higher in smokers as compared to non-smokers even before creation of pneumoperitoneum, which is due to the compromised lung function following chronic smoking. This condition gets aggravated after creation of pneumoperitoneum which is very much evident from the serial arterial blood gas analysis. The level of CO2 remains elevated even after deflation of the pneumoperitoneum. Hence one has to be very much vigilant not only during intra-operative period but also in post-operative care unit. Hence serial ABG monitoring should be included as a part of the protocol especially in laparoscopic surgeries.

NCT ID: NCT03018964 Not yet recruiting - Clinical trials for Cholecystectomy, Laparoscopic

Solo Single Incision Laparoscopic Cholecystectomy

Start date: March 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine safety of solo surgery in single incision laparoscopic cholecystectomy (SILC) with a camera holder comparing to a camera operator assisted SILC

NCT ID: NCT02978989 Not yet recruiting - Clinical trials for Cholecystectomy, Laparoscopic

Solo and Non-solo Approach for Laparoscopic Cholecystectomy

SOLOGB
Start date: December 2016
Phase: N/A
Study type: Interventional

To determine the safety and feasibility of solo laparoscopic cholecystectomy, which is defined as the application of solo surgery to laparoscopic cholecystectomy, by comparing consecutive non-solo procedures conducted by a surgeon in the presence or absence of human assistant(s).

NCT ID: NCT02575443 Completed - Clinical trials for Cholecystectomy, Laparoscopic

Neuromuscular Block and Anesthetic Depth Monitoring

Start date: September 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluated whether the depth of neuromuscular block may affect the unicon value of anesthetic depth monitoring system (ADMS).

NCT ID: NCT02185716 Completed - Pain, Postoperative Clinical Trials

Transversus Abdominis Plane Block (TAP) for Laparoscopic Cholecystectomy Surgery

Start date: January 2014
Phase: Phase 4
Study type: Interventional

Postoperative pain is a significant cause of increased morbidity in the perioperative period, leading to patient discomfort and greater hospital length of stay. Laparoscopic cholecystectomy associated with significant postoperative pain, a substantial component of which is derived from abdominal wall incisions. Ultrasound-guided TAP block increasingly has been used for providing pain relief following abdominal surgery. We designed this study with the hypothesis that, administering TAP block with levobupivacaine in laparoscopic cholecystectomy provides superior analgesic effects than port-side infiltration.

NCT ID: NCT01523886 Completed - Clinical trials for Cholecystectomy, Laparoscopic

The Muscle Relaxation-study

Start date: March 2012
Phase: Phase 4
Study type: Interventional

The purpose of this investigation is to compare the surgical conditions during laparoscopic cholecystectomy at a low intra-abdominal pressure with deep or moderate muscle relaxation. The primary hypothesis is that surgical conditions during laparoscopic cholecystectomy are better with deep muscle relaxation than moderate muscle relaxation.

NCT ID: NCT01094379 Recruiting - Clinical trials for Cholecystectomy, Laparoscopic

A Randomised Comparison Between Single Incision Laparoscopic Cholecystectomy and Standard Laparoscopic Cholecystectomy

Start date: April 2010
Phase: N/A
Study type: Interventional

Laparoscopic cholecystectomy has been established as the treatment of choice for symptomatic gallstone disease. The main advantages of laparoscopic surgery are the cosmetic result, reduced postoperative pain, shorter hospital stay and rapid return to normal activity. Although reduced, however, pain is still substantial and constitutes the main clinical problem after laparoscopic cholecystectomy, especially for planned day case procedures. Recently, a new technique of laparoscopic cholecystectomy has been developed, in which all instruments are inserted through the same umbilical incision. The single incision laparoscopic surgery (SILS) technique for cholecystectomy has been proved to be feasible and safe by several studies. The purpose of the study is to compare postoperative pain and operating time, nausea, vomiting, tissue damage, pulmonary function, cosmetic result, quality of life between SILS and standard laparoscopic cholecystectomy.