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Laparoscopic Cholecystectomy clinical trials

View clinical trials related to Laparoscopic Cholecystectomy.

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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: NCT02469831 Completed - Clinical trials for Laparoscopic Cholecystectomy

Respiratory Mechanics and Metabolic Changes During Low Pressure Laparoscopic Cholecystectomy

Start date: October 2014
Phase: Phase 2
Study type: Interventional

The investigators aim to investigate the differences between deep continuous muscle relaxation and moderate blockade during low-pressure (8 mmHg) laparoscopic cholecystectomy in respect to metabolic changes and respiratory mechanics.

NCT ID: NCT02071550 Completed - Clinical trials for Laparoscopic Cholecystectomy

10cmH2O Peep Application and Cerebral Oxygenation in Laparoscopic Surgery: a Comparative Study With Invos and Foresight Devices

NIRS AND PEEP
Start date: August 2013
Phase: N/A
Study type: Observational [Patient Registry]

In this study the investigators investigated changes in hemodynamic parameters and cerebral oxygen saturation (rSO2) associated with 10 cmH2O PEEP, which is assumed beneficial for the respiratory functions and oxygenation during the laparoscopic cholecystectomy (LC) applied at the 30°head-up left side position, is compared with using two individual devices (INVOS-FORESIGHT). Methods: Afterwards the ethics committee approval of the hospital and receiving the written patients' consents, patients to undergo ASA I-II group elective laparoscopic surgery were randomly divided into two groups. Sensors of INVOS and FORESIGHT devices were placed on the right side forehead region. Totally 11 evaluation periods were formed, respectively: Pre-induction (1st Period), post-induction (2nd period), abdominal insufflation outset (3rd period): post-insufflation 5-minute intervals (4th, 5th, 6th, 7th 8th period), end of insufflation (9th period), end of operation (10th period) and end of anaesthesia (11th period). While one of the groups was not applied PEEP(ZEEP), the other group was applied 10 cmH2O simultaneously with the abdominal insufflation proceeding. Demographic data, hemodynamic values and rSO2 values were recorded for both groups at all 11 periods.

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.

NCT ID: NCT01685775 Completed - Clinical trials for Laparoscopic Cholecystectomy

Needlescopic Versus Transvaginal/Transumbilical Cholecystectomy

NATCH
Start date: February 2010
Phase: N/A
Study type: Interventional

Laparoscopic surgery has become the golden standard for the removal of the gallbladder. Recently, developments have been made so that operations can be performed through a natural orifice instead of the abdominal wall, thus minimizing the trauma of a procedure. This study compares the transvaginal/transumbilical cholecystectomy with the laparoscopic operation using 2-3mm instruments in female patients. It also examines the benefits and disadvantages related to postoperative pain, cosmetic aspects, and potential physiological alterations to the transvaginal approach that affect sexual intercourse.

NCT ID: NCT01595165 Recruiting - Postoperative Pain Clinical Trials

Transversus Abdominis Plane Block and Postoperative Pain After Laparoscopic Cholecystectomy

Start date: July 2012
Phase: N/A
Study type: Interventional

Transversus abdominis plane (TAP) block has gained popularity for the control of postoperative pain in various surgeries. Three studies showed inconsistent result on pain control after TAP block in laparoscopic cholecystectomy. The TAP technique used in these studies was classic ultrasound guided TAP block. Besides periumbilical incision, sub-xiphoid incision is usually made during laparoscopic cholecystectomy. As typical posterior TAP rarely extend above T8, the investigators undergo subcostal TAP block for this type of surgery. The investigators are going to investigate the effect of subcostal TAP on early postoperative pain after laparoscopic cholecystectomy.

NCT ID: NCT01398683 Enrolling by invitation - Clinical trials for Laparoscopic Cholecystectomy

Comparison Epidural Anesthesia and General Anesthesia in Laparoscopic Cholecystectomy

Start date: April 2011
Phase: N/A
Study type: Observational

Comparison of epidural anesthesia and general anesthesia for laparoscopic cholecystectomy, patients in the surgery and the effectiveness of anesthesia after surgery, the incidence of side effects or complications, and postoperative recovery of the body of the differences

NCT ID: NCT01312025 Completed - Clinical trials for Laparoscopic Cholecystectomy

Conventional Versus Modified Laparoscopic Cholecystectomy

Start date: n/a
Phase: N/A
Study type: Interventional

In conventional laparoscopic cholecystectomy, the cystic duct and artery are clipped by metal clips. we propose a new method in which the cystic duct is ligated and the cystic artery is cauterized. the investigators compare both methods.

NCT ID: NCT01269099 Completed - General Anesthesia Clinical Trials

Hypokalemia and Intravenous Patient Controlled Analgesia

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

The increase in stress hormone level and hyperventilation caused by the postoperative pain may contribute to the development of hypokalemia during postoperative period. Therefore, if the postoperative pain is well controlled by the IV-PCA,the plasma potassium level during the postoperative period may be not affected by stress response. The researchers tried to investigate the effect of IV-PCA on potassium regulation during the postoperative period.

NCT ID: NCT01267916 Completed - General Anesthesia Clinical Trials

Intrinsic PEEP During Mechanical Ventilation of Patients With Obesity

Start date: January 2011
Phase: N/A
Study type: Interventional

It is demonstrated that expiratory flow limitation and as a consequence, intrinsic positive end-expiratory pressure (PEEP) is present in grossly obese subjects especially in the supine position. The investigators tried to investigate the effect of low respiratory rate and high tidal volume on the intrinsic PEEP and gas exchange for obese subjects undergoing general anesthesia.