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Laparoscopy clinical trials

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NCT ID: NCT02781194 Completed - Postoperative Pain Clinical Trials

Temperature and Pain in Laparoscopy

TePaLa
Start date: July 2016
Phase: N/A
Study type: Interventional

The aim of this investigation is to assess the impact of forced air warming, warm humidified insufflation gas and the combination of the two on intraoperative temperature maintenance and the postoperative pain course as well as the fibrinolytic activity in peritoneal fluid following laparoscopic procedures (duration > 60 min) in a prospective, randomized, controlled, mono-centric study. Therefore 150 subjects will be randomized in 3 groups of 50 subjects each. First group will be treated with forced-air warming blanket (bair hugger). Second group will be treated with warmed, humidified insufflation via the F&P HumiGardâ„¢ Surgical Humidification System. Third group will be treated with both, warming blankets and warmed, humidified insufflation. The peri-operative temperature of patients might be higher in patients of the third group with the combination of both treatments. The investigators hypothesize that VAS scores for pain (especially shoulder pain), and MEDD usage will differ between groups. Wound infection incidence and time spent in PACU are also expected to differ. Fibrinolytic activity in the peritoneal fluid is expected to be higher in patients undergoing laparoscopic procedures with humidified gas insufflation, since the trauma to the peritoneum will be less.

NCT ID: NCT02773173 Completed - Laparoscopy Clinical Trials

Individualized Pneumoperitoneum Pressure in Colorectal Laparoscopic Surgery Versus Standard Therapy (IPPCollapse-II)

Start date: January 25, 2017
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the post-operative recovery quality of the Individualized Pneumoperitoneum Pressure Therapy in Colorectal laparoscopic surgery versus standard therapy using a quality validated scale of postoperative recovery of their stay in the Post-Anaesthesia Recovery Unit.

NCT ID: NCT02685007 Completed - Laparoscopy Clinical Trials

RollOut -Pre-Rolled TachoSil in Laparoscopic Utilisation. A Non-Interventional Study

Start date: April 5, 2016
Phase:
Study type: Observational

The purpose of this study is to describe ease of use and satisfaction with application of the pre-rolled TachoSil in laparoscopic procedures within approved therapeutic indication as per Summary of Product Characteristics (SmPC).

NCT ID: NCT02527967 Completed - Colonic Neoplasms Clinical Trials

ERAS in Laparoscopic Surgery for Colorectal Cancer: Risk Factors for Delayed Recovery

Start date: January 2013
Phase: N/A
Study type: Observational

Although there is evidence for reducing complication rate and improving recovery after the implementation of Enhanced Recovery After Surgery (ERAS) protocols into colorectal surgery, most published papers include patients undergoing open resections. The aim was to analyse factors affecting recovery and length of stay (LOS) in patients after laparoscopic colorectal surgery for cancer combined with ERAS protocol.

NCT ID: NCT02511652 Completed - Laparoscopy Clinical Trials

Ambu AuraGain vs LMA Supreme in Laparoscopic Surgery

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

The aim of the study is to compare the performance of two supraglottic airway devices (SGA), the new Ambu AuraGain and the LMA Supreme, in sixty female patients undergoing gynaecologic laparoscopy in the trendelemburg position. Primary outcome is the airway seal pressure. Secondary outcomes are ease of insertion, quality of ventilation, endoscopic view of the glottis, gastric tube passage and complications.

NCT ID: NCT02505724 Completed - Laparoscopy Clinical Trials

Peer-coaching to Teach Faculty Surgeons an Advanced Laparoscopic Skill

Start date: July 2014
Phase: N/A
Study type: Interventional

This single-blinded randomized controlled trial assesses the efficacy of peer-coaching to teach novice surgical faculty an advanced laparoscopic skill.

NCT ID: NCT02185339 Completed - Laparoscopy Clinical Trials

Effects of Deep Neuromuscular Blockade on Intraoperative Respiratory Mechanics

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

The primary objective of the current study is to compare intraoperative respiratory mechanics in patients receiving laparoscopic renal surgery under deep neuromuscular blockade (dNMB) and under moderate neuromuscular blockade (mNMB). In addition, we will compare intraoperative hemodynamics and postoperative pulmonary function between the two groups.

NCT ID: NCT02085902 Completed - Laparoscopy Clinical Trials

Does the Use of Ropivacaine Facilitates Cholecystectomy by Laparoscopy in Ambulatory Surgery?

VesiRop
Start date: March 2014
Phase: Phase 4
Study type: Interventional

Since the recommendations of the French Society of Digestive Surgery 2010, cholecystectomy can be performed as outpatient surgery. This approach is difficult in many centers because of post operative pain and nausea/vomiting. The use of postoperative morphine may be responsible for the state of nausea. The use of ropivacaine allows a reduction of the morphine consumption and thus may allow the patient to have their surgery as an outpatient. Currently, ropivacaine is used randomly during the investigators surgeries. Initially, it was used for the infiltration holes trocar. In recent years, ropivacaine is used for the reduction of intra-abdominal postoperative pain. Its use is made of parietal surgery ( hernia ) in cholecystectomy and colonic surgery. This mode of administration is allowed to view the many publications made on this subject. Its use in the investigators daily surgery, however, has not been evaluated in ambulatory surgery.

NCT ID: NCT02079337 Completed - Clinical trials for Neuromuscular Blockade

Validation of Subjective Rating Scales Used to Assess Surgical Conditions in Abdominal Surgery

Start date: November 2013
Phase: Phase 4
Study type: Interventional

Use of neuromuscular blockade (NMB) may improve the surgical work space in patients scheduled for laparoscopic surgical cases (e.g. hysterectomy, ovarian cystectomy, myomectomy). Clinical studies investigating this question often use a numerical or verbal rating scale for subjective evaluation of the surgical workspace. However, no good subjective rating scale have been developed or validated. Neither have possible inter-individual differences in use of such subjective scales been described. Purpose: The aim of this study is to validate different subjective rating scales to determine which scale is most useful among surgeons.

NCT ID: NCT02025075 Completed - Clinical trials for Postoperative Complications

Hemodynamic and Respiratory Variations During Laparoscopic Surgery With and Without Deep Neuromuscular Blockade.

Start date: January 2014
Phase: N/A
Study type: Interventional

The goal of this study is to investigate the effect of depth of neuromuscular block (NMB) on global and regional (dependent versus nondependent) respiratory mechanics during laparoscopic surgery. Furthermore, we will investigate if the level of NMB influences intraoperative hemodynamic and cerebral oxygenation.