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Laparoscopic Cholecystectomy clinical trials

View clinical trials related to Laparoscopic Cholecystectomy.

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NCT ID: NCT05158270 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Erector Spinae Plane Block As Alternative Analgesic Modality in Laparoscopic Cholecystectomy

Start date: November 15, 2021
Phase: N/A
Study type: Interventional

Adequate analgesic regimen is one of the most important key elements of Enhanced recovery after surgery (ERAS) protocols. The cornerstone of analgesia is multimodal analgesia combining local anesthetic (LA) techniques and trying to avoid parenteral opioids and their side effects. Subcostal approach to Anterior quadratus lumborum block (SAQLB), compared to other variants of quadratus lumborum blocks (QLBs), was associated with wider and longer sensory blockade, and provided somatic as well as visceral analgesia of the abdomen. The newly emerging, relatively easy erector spinae plane block (ESPB) provided excellent analgesia across a variety of surgical procedures and reduced opioid consumption. This motivated us to do this study to assess and compare the analgesic efficacy of ESPB versus SAQLB following laparoscopic cholecystectomy.

NCT ID: NCT05094193 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Trocar-site Infiltration Versus TAP-block

Start date: October 1, 2021
Phase: N/A
Study type: Interventional

For symptomatic gall bladder disorders (cholelithiasis and cholecystitis), laparoscopic cholecystectomy (LC) has been considered as the gold standard treatment. However, these minimally invasive technique is associated with acute moderate pain during the 24 hours postoperative, which is routinely managed using opioids. The transversus abdominis plane (TAP) block has been used as part of a multimodal analgesia strategy. Besides, Wang et al found that TAP block is more effective than a conventional pain control, but not significatively different from another local incisional pain control that is port site infiltration.So, the aim of this study, is to compare the analgesic efficacy and safety of trocar-site infiltration with ropivacaine with ultrasound-guided TAP block following laparoscopic cholecystectomy when used as part of multimodal analgesia.

NCT ID: NCT05079880 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Effect of Caffeine on Time to Anesthetic Emergence After Laparoscopic Cholecystectomy : Randomized-controlled Trial

Start date: August 15, 2021
Phase: Phase 2
Study type: Interventional

A faster emergence from general anesthesia has a double medico-economic impact by reducing the risks of complications and optimizing the performance of surgical units. No drug has been retained for its ability to actively accelerate anesthetic emergence by antagonizing hypnotics. Thus, the aim of this study was to examine the effect of caffeine on the time to emerge from sevoflurane anesthesia for laparoscopic cholecystectomy.

NCT ID: NCT05002426 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Rouviere Sulcus Plane and Hepatic Hilum Plane, Which is Better as a Landmark in Laparoscopic Bile Duct Surgerys

Start date: January 4, 2021
Phase:
Study type: Observational

RS and the RS plane are important anatomical markers in laparoscopic cholecystectomy. However, there are many variations in the shape and orientation of the RS, and the RS plane is an imaginary plane, which can be misjudged by different surgeons. The purpose of this study is to introduce a more intuitive anatomical marker and anatomical plane, hilum plane, and discuss the application value of hilum plane in laparoscopic biliary surgery by comparing it with RS and RS plane.

NCT ID: NCT04888117 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Prospective Multi-Center Study of Short-Term Outcomes After Complex Cholecystectomy

Start date: June 5, 2021
Phase:
Study type: Observational

The study aims to evaluate the short-term clinical outcomes after complex robotic-assisted and laparoscopic cholecystectomies.

NCT ID: NCT04162106 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Feasibility of the Ultravision™ System in Low Pressure Laparoscopic Cholecystectomy Compared to Airseal® IFS

Start date: November 2019
Phase: N/A
Study type: Interventional

This post-market clinical study is designed to evaluate the effectiveness of the Ultravision™ System when compared to the Airseal® iFS within an approved indication for use, namely laparoscopic cholosystectomy.

NCT ID: NCT04138472 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Comparison Of Dexmedetomidine, Fentanyl And Lignocaine In Attenuation Of Hemodynamic Response To Direct Laryngoscopy And Intubation In Patient Undergoing Laparoscopic Cholecystectomy

Start date: October 30, 2019
Phase: N/A
Study type: Interventional

Comparison Of Dexmedetomidine, Fentanyl And Lignocaine In Attenuation Of Hemodynamic Response To Direct Laryngoscopy And Intubation In Patient Undergoing Laparoscopic Cholecystectomy

NCT ID: NCT03836170 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Analysis of the Impact of Cholecystectomy on Gut Microbiome in Adults

Start date: May 15, 2018
Phase: Phase 1
Study type: Interventional

Laparoscopic cholecystectomy (LC) is widely used in the gallbladder stone, gallbladder polyp, gallbladder cancer and other diseases. Some of the patients would develop diarrhea after surgery, and studies have reported an increased risk of colorectal cancer after LC. The aim of the present study was to examine the effects of LC on the gut microbiota.

NCT ID: NCT02768376 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Spinal for Laparoscopic Cholecystectomy

Sp-Lap
Start date: March 2016
Phase: N/A
Study type: Interventional

In this study, the investigators will study spinal anesthesia for laparoscopic cholecystectomy in comparison to general anesthesia (GA) regarding patient satisfaction as a primary variable, intraoperative complications, postoperative analgesic requirements, postoperative nausea and vomiting, patient hospital stay (secondary variables).

NCT ID: NCT01823224 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

A Prospective, Randomized, Double Blind, Comparative-effectiveness Study Comparing Perioperative Administration of Oral Versus Intravenous Acetaminophen for Laparoscopic Cholecystectomy

Start date: February 2013
Phase: N/A
Study type: Interventional

The purpose of the study is to learn whether perioperative IV (intravenous) administration of acetaminophen (commonly referred to as Tylenol) shows any different clinical outcomes over the oral (by mouth) administration of acetaminophen for a patient having a laparoscopic cholecystectomy. If improved pain scores occur with the administration of IV acetaminophen, it may result in fewer requests for pain-related intervention such as other oral pain medications.