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Pneumoperitoneum clinical trials

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NCT ID: NCT01740011 Completed - Hernia Clinical Trials

Prospective Randomized Trial on Comparison of Standard- Carbon Dioxide Pressure Pneumoperitoneum Insufflators Versus AirSeal

AirSeal
Start date: January 2013
Phase: N/A
Study type: Interventional

The primary objective of the present trial is to investigate, the mean operative time and to study the frequency and intensity of postoperative shoulder tip pain in patients undergoing laparoscopic surgery, i.e. cholecystectomy, colorectal surgery, hernia repair with AirSeal® compared with standard pressure CO2 insufflation systems. The primary hypothesis is that patients operated with AirSeal® have a shorter mean operative time and decreased frequency and intensity of postoperative shoulder tip pain compared with patients undergoing surgery with standard pressure CO2 insufflation systems. It is the secondary objective of the trial to evaluate immunologic and anaesthesiological aspects of laparoscopic cholecystectomy, colorectal surgery and laparoscopic hernia repair by observing the immune responses and volume of mechanical ventilation of the two groups through measuring various immunologic factors and ventilation volume/CO2 elimination volume. Surgical side effects will also be measured as secondary objective.

NCT ID: NCT01512511 Completed - Pneumoperitoneum Clinical Trials

Comparing Nitrous Oxide and Carbon Dioxide for Laparoscopic Cholecystectomy

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

There is no general agreement about the ideal gas for pneumoperitoneum. CO2, now in common use, has not compared to N2O sufficiently to disclose which one has minimal "physiological" invasiveness characters. Assigned randomly to carbon dioxide or nitrous oxide group, the hemodynamic and respiratory parameters (heart rate, mean arterial blood pressure, end-tidal CO2, minute ventilation, and O2 saturation) before pneumoperitoneum and during it were recorded. Pain, as perceived by patients, is measured 2, 4 and 24 hours after the procedure by visual analogue scale. Vomiting and use of analgesics and antiemetics were recorded and compared.

NCT ID: NCT01344499 Completed - Clinical trials for Laparoscopic Hysterectomy

Clearance Rate of Peritoneal Fluid After Full Conditioning Pneumoperitoneum

Start date: August 2009
Phase: N/A
Study type: Interventional

Measurement of residual peritoneal fluid after laparoscopic surgery

NCT ID: NCT01340989 Completed - Pneumoperitoneum Clinical Trials

CO2 Absorption During Laparoscopy

Start date: August 2006
Phase: N/A
Study type: Interventional

CO2 absorption from the pneumoperitoneum increases over time during laparoscopic procedures. Adding 4% of oxygen to the carbon dioxide was shown in rabbits to decrease CO2 resorbtion through prevention of mesothelial hypoxia. We want to prove this concept in human and expand it to the use of full conditioning.

NCT ID: NCT01289379 Completed - Cholecystolithiasis Clinical Trials

The Effect of High Frequency Jet Ventilation (HFJV)During Laparoscopic Operations

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

Investigators conducted a randomised perspective study to determine whether the use of HFJV instead of conventional mechanical ventilation will reduce the adverse cardiovascular effects of pneumoperitoneum during laparoscopic surgery.

NCT ID: NCT01009372 Completed - Stress Physiology Clinical Trials

The Intermittent Pneumoperitoneum Scheme of Work Breaks in Complex Laparoscopic Surgery

IPP
Start date: January 2007
Phase: N/A
Study type: Interventional

Many people spanning from air traffic controllers to simple production line workers share regular compulsive breaks to revert fatigue whilst they work. This is uncommon for medical operators - a macho image is still as prevalent in real life as it is in countless TV series. We report on the first clinical trial on regular intraoperative breaks. For one time we turned our scientific curiosity to ourselves. This included the intraoperative collection of body fluids and required transparency which was not easy to obtain. It was rewarded with striking results: Regular intraoperative breaks lowered significantly the operators stress hormone levels, improved error-performance testing results and musculoskeletal fatigue scores. Subjectively the breaks enhanced the practitioners satisfaction. Surprisingly the operator's breaks were not at the cost of the patient: because the did not prolong the overall operation time at all and - in our setting- they significantly increased of cardiac output and urine production.

NCT ID: NCT00678366 Completed - Pain Clinical Trials

Evaluation of Adding Small Amounts of Oxygen to the CO2 Pneumoperitoneum Upon Pain and Inflammation

Start date: May 2008
Phase: Phase 3
Study type: Interventional

The study intends to investigate the use of a novel gaz-composition used during laparoscopy upon pain and inflammation in the post-operative period.

NCT ID: NCT00606762 Completed - Cholelithiasis Clinical Trials

Comparison Between Low Pressure Versus High Pressure Laparoscopic Cholecystectomy

Start date: October 2006
Phase: N/A
Study type: Interventional

The physiological changes and postoperative pain are directly related with the degree of intra-abdominal pressure kept during the laparoscopy. The present study aims to examine difference between low pressure pneumoperitoneum (8 mm Hg)and High pressure pneumoperitoneum (12 mm Hg)during laparoscopic cholecystectomy in terms of pain, cardio-pulmonary function, arterial blood gas changes etc.

NCT ID: NCT00567125 Completed - Laparoscopy. Clinical Trials

Comparison of Systemic Response After Laparoscopies Performed With Standard and Low-Pressure Pneumoperitoneum

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of the study was the comparative assessment of the influence of low and standard pressure CO2 pneumoperitoneum on the systemic inflammatory and angiogenic responses during the postoperative period after laparoscopic management of cholelithiasis.