CholecystitisNCT02264444
Establishing Visualization Grading Scale on LESS Cholecystectomy
A study testing Cholecystectomy visualization in people with Cholecystitis, run by Florida Hospital Tampa Bay Division at 1 site in United States.
Trial summary
Essential to laparoscopic operations is adequate visualization. Unfortunately there is no grading system to assess the degree or quality of visualization. The primary objective of the project is to develop a laparoscopic visualization scoring system. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Cholecystitis
- What is being tested?
- Cholecystectomy visualization
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 30 participants
- Where
- 1 siteUnited States
- Study dates
- Sep 2013to Aug 2016
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Signed informed consent
- 18 years of age and older
- All patients deemed to have a clinical and surgical indication to undergo a LESS cholecystectomy
Who cannot join
- Pregnancy
- Breastfeeding
- BMI>35
- Serious comorbidities precluding a LESS cholecystectomy
- Known or suspected neuromuscular disorders impairing neuromuscular function
- Allergies to muscle relaxants, anesthetics or narcotics utilized for this study
Show all 11Show fewer
- A (family) history of malignant hyperthermia
- A contraindication for neostigmine administration
- Chronic opioid use
- Prolonged QT syndrome
- Creatinine >2.0
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Grading System for Laparoscopic Visualization and Predicting Factors That Affect Visualization Level During Laparoscopic Cholecystectomies: A Prospective, Single Group, Open Label Study
Essential to laparoscopic operations is adequate visualization. Unfortunately there is no grading system to assess the degree or quality of visualization. The primary objective of the project is to develop a laparoscopic visualization scoring system. We also intend to investigate the effects of neuromuscular blockade agents on visualization.
Read the detailed description
Essential to laparoscopic operations is adequate visualization. Unfortunately there is no grading system to assess the degree or quality of visualization. There are many contributing factors that either assist or hinder the quality. Compared to open surgical procedures, laparoscopic surgical procedures (Laparo-endoscopic Single Site (LESS) and conventional multiport) are associated with less postoperative pain, a lower wound infection rate, shorter length of hospital stays and reduced incidence of late ventral hernia(1). Despite these well documented benefits of laparoscopic procedures, laparoscopy in certain patient populations can be challenging. Preoperative factors that contribute to technical difficulty in performance of laparoscopic procedures include male gender, android body habitus, and body mass index (BMI) greater than 30 kg/m2(2). Men often have an android body habitus, whereby the excess body fat concentrates within the peritoneal cavity, increases intra-abdominal pressure and thus reduces intraoperative laparoscopic visualization. Intra-abdominal pressure measured in morbidly obese patients is 2-3 times higher than in non-obese patients. In addition, android body habitus and high BMI are often associated with an enlarged left lobe of the liver. These factors can contribute to the degree of intraoperative technical difficulty and should be weighed in selection of appropriate patients to undergo laparoscopic procedures.
Particularly in the early period of the surgeon's learning curve, we suggest that selection criteria for laparoscopic procedures for the upper abdomen be limited to patients with a low BMI and no previous upper abdominal surgery. Although low BMI is a relatively good predictor of a less challenging laparoscopic procedure, a high BMI does not necessarily predict intraoperative technical difficulty. We predict that the best method to determine the technical difficulty of laparoscopic procedures is during intraoperative evaluation. For example, the primary limiting factor in determining the technical difficulty of laparoscopic Roux-en-Y gastric bypass (RYGBP) is the size and thickness of the left lobe of the liver. A massively enlarged left lobe of the liver obscures the laparoscopic view of the gastro-esophageal junction and angle of His, making the gastrojejunal anastomosis difficult to construct. Schwartz et al. support this concept when they found that a large liver was the primary reason for conversion from laparoscopic to open RYGBP in an analysis of 1,000 patients (2).
A laparoscopic operation consists of making small punctures into the peritoneum, through which, a camera and surgical instruments are subsequently inserted. The laparoscopically placed camera is the only view of the operative field. Since this point of view is constantly changing to meet the surgeon's needs during the operation, and because it is very different from the exoscopic view of the surgeon, the surgeon has to be very well trained to interpret the images through the laparoscopic view. For LESS operations, a deflectable tip laparoscope is utilized in aiding the surgeon for improved visibility and less clashing of instruments.
The laparoscopic view does not reveal, at one time, all the structures the surgeon needs to see in order to complete the surgical procedure with success. These structures can, for instance, be hidden behind the peritoneal wall (e.g., the ureter). This limitation cannot only lead to a less efficient operation, but can also lead to complications. Often such structures can be extracted from preoperative CT/MR images; however, the surgeon needs to interpret and fuse these images with the laparoscopic view. To alleviate this problem, we propose a laparoscopic visualization scoring system based on the intraoperative quality of images (3).
The impact of muscle relaxants on the isolated abdominal wall or diaphragmatic behavior and the absolute intra-abdominal volume are difficult to measure. Conversely, the inflated volume-pressure relationship of the abdominal cavity is easier to measure. A description of this volume-pressure relationship has not been identified in previous studies. Clinical data supports a positive linear correlation between the depth of neuromuscular blockade and abdominal wall and diaphragmatic relaxation and compliance (4). There is a very tangible and real effect of the neuromuscular blockade; this ultimately has a direct impact on the quality of visualization of the surgical field during a laparoscopic procedure (5). A constant neuromuscular block leads to preferable working conditions for the surgeon. The evoked muscle responses after neurostimulation can be registered by electromyography (EMG), mechanomyography (MMG) and acceleromyography (AMG). In principle, different peripheral nerves can be used for neurostimulation. The EMG records the electrical signal generated by the muscular action potential under its surface electrodes. The force of the thumb after stimulation can be registered by MMG. The AMG records the acceleration of the thumb after neurostimulation. The EMG, MMG and AMG system allows for observation of the measured signals quantity and quality (6).
We have identified other relevant factors that significantly affect the quality of visualization during different laparoscopic procedures including:
- Clarity, focus and brightness: The laparoscope typically consists of an outer ring of optical fibers used to transmit light into the body, and an inner core of rod lenses that illuminate visual scene. This is then relayed back to the camera. Various different types of laparoscopes are available; they are specified in terms of overall length, number of rods, diameter and angle of view. Generally speaking, the wider the scope the brighter the resulting image. Lenses are available in the range of 1.9mm to 12mm, but sizes of 5mm and 10mm are the most common choices for pediatric and adult patients, respectively.
- Breadth of intra-abdominal field and vertical space measured in centimeters: Breadth of intra-abdominal field and vertical space are factors directly related to pressure insufflation as well as the level of the neuromuscular blockade.
- Distracting factors: This specific category of distracting factors includes:
- Blood: the presence, especially in large quantities, may prevent adequate visualization.
- Smoke: unipolar electrocautery and/or the bipolar Maryland forceps produce smoke when used. The rate of aspiration and evacuation also affect visualization.
- Adhesions: the presence of intra-abdominal adhesions, which hinders and prohibits proper identification of the anatomic structures.
- Sterile iodine impregnated covering sheet: its application presumably has a negative impact on abdominal wall and diaphragmatic compliance, and therefore, may obscure visualization.
- Intra-intestinal air: the presence of air inside the stomach, and small and large intestines adversely affects the size of the visual field. This can be prevented by an adequate preoperative bowel preparation and placement of an aspiration NG tube during anesthesia induction.
- Patient's specific factors such as BMI value and body habitus: From our experience, a BMI under 26 allows for optimal field visualization. Conversely, a BMI greater than 26 negatively impacts the visual field. However, a recent study conducted by Camani et al. in 2010 showed that the laparoscopic approach in the various applications of gynecologic surgery is not significantly influenced by BMI in terms of surgical outcomes, laparotomy conversion rate, intraoperative and postoperative complication rate, and duration of hospital stay (4). We feel that visualization during operations involving the abdominal cavity are adversely affected by high amounts of adipose tissue, and therefore, a visualization scoring system will help support this theory.
- Type of disorder (malignant vs. benign) that the laparoscopic procedure is undertaken for: Due to many pathologic factors such as the need for R0 resections, the discovery of more advanced disease than anticipated, the presence of adhesions or scar tissue from previous operations, laparoscopic procedures for malignant disorders may require a better visualization field than laparoscopic procedures undertaken for benign disorders.
- Inadequate and/or poorly designed instruments: Most laparoscopic instrument development is technology-driven. This approach to instrument design does not always consider the ergonomics of the users, therefore leading to a user-unfriendly product (4, 5).
- Technical difficulties: An intraoperative technical difficulty is defined as a significant deviation from the ordinary surgical procedure. All conversions to an open operation and iatrogenic bowel perforation during laparoscopic surgery are examples of technical difficulties. Many studies demonstrate that a technical difficulty during laparoscopic-assisted surgery jeopardizes both the intra-operative and postoperative patient safety.
- Patient's body position during laparoscopic procedure:
A study led by Mulier, J et al. in 2010 demonstrated that the Trendelenburg position for lower abdominal surgery and reverse Trendelenburg with flexing of the legs at the hips for upper abdominal surgery effectively improved the workspace in obese patients, even with full muscle relaxation (6).
II. Objectives A.Primary Objective The primary objective is to develop a laparoscopic visualization scoring system.
- Secondary Objectives
The secondary objectives are:
- To determine how visualization is affected by various levels of pneumoperitoneum correlated with neuromuscular blockade.
- Identify the factors that influence visualization, and determine how to manage these factors to optimize visualization.
- Determine if there is a statistically significant correlation between different degrees of visualization and the following intraoperative time intervals:
- surgical incision to sterile wound dressing
- sterile wound dressing to extubation
- sterile wound dressing to patient exiting operating room
- Determine if there is a statistically significant correlation between different degrees of visualization and postoperative pain.
- Conditions
- Cholecystitis
- Being tested
- Cholecystectomy visualization
- Keywords
- Cholecystectomy, visualization, single incision
- Medical subject headings
- Cholecystitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Cholecystectomy visualizationOther
Patients undergo a standard removal of the gallbladder through a single incision at the umbilicus will have their operation recorded and graded according to a scale that is established for this study.
| Study group | Role | What they receive |
|---|---|---|
| Cholecystectomy visualization | Experimental | All patients will undergo a standard single site cholecystectomy and will have their operation recorded and scored for visualization. Receives: Other: Cholecystectomy visualization |
What is being measured
The primary outcome is the main question the study is designed to answer.
Laparoscopic Visualization Score assessment
Measured: Start to end of LESS Cholecystectomy
Secondary outcomes (4)
pneumoperitoneum volume
Measured: start to end of LESS cholecystectomy
factors influencing visualization
Measured: start to end of LESS cholecystectomy
Degrees of visualization
- surgical incision to sterile wound dressing
- sterile wound dressing to extubation
- sterile wound dressing to patient exiting operating room
Measured: start to end of LESS cholecystectomy
postoperative pain
Measured: every day until 7 days after LESS cholecystectomy
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted15 Oct 2014 (estimated)
- Study startSep 2013
- Primary completionJun 2016
- Study completionAug 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (7)Papers the sponsor has linked to this study.
- Other trials for CholecystitisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 30 participants (actual)
Sponsor and investigators
- Lead sponsor
- Florida Hospital Tampa Bay Division
- Sponsor type
- University, hospital or other
- Collaborators
- Merck Sharp & Dohme LLC
- Responsible party
- Principal investigator, Alexander Rosemurgy, Florida Hospital Tampa Bay Division
- Investigators
- Alexander S. Rosemurgy, MD, Principal investigator, Florida Hospital Tampa Bay Division
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02264444
- Sponsor's protocol ID
- 461326
- Status last verified
- Jul 2017
- First submitted
- 1 Oct 2014
- Last updated
- 28 Jul 2017
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No
Publications
Schrenk P, Woisetschlager R, Rieger R, Wayand WU. A diagnostic score to predict the difficulty of a laparoscopic cholecystectomy from preoperative variables. Surg Endosc. 1998 Feb;12(2):148-50. doi: 10.1007/s004649900616.
PubMed 9479730Nguyen NT, Longoria M, Gelfand DV, Sabio A, Wilson SE. Staged laparoscopic Roux-en-Y: a novel two-stage bariatric operation as an alternative in the super-obese with massively enlarged liver. Obes Surg. 2005 Aug;15(7):1077-81. doi: 10.1381/0960892054621062.
PubMed 16105411Stijn de Buck, Johan van Cleynenbreugel, Indra Geys, Thomas Koninckx, Philippe R Koninck, Paul Suetens. A System to Support Laparoscopic Surgery by Augmented Reality Visualization. Medical Image Computing and Computer-Assisted Intervention; 691-8, 2001.
Camanni M, Bonino L, Delpiano EM, Migliaretti G, Berchialla P, Deltetto F. Laparoscopy and body mass index: feasibility and outcome in obese patients treated for gynecologic diseases. J Minim Invasive Gynecol. 2010 Sep-Oct;17(5):576-82. doi: 10.1016/j.jmig.2010.04.002. Epub 2010 Jul 8.
PubMed 20619751McDougall EM, Figenshau RS, Clayman RV, Monk TG, Smith DS. Laparoscopic pneumoperitoneum: impact of body habitus. J Laparoendosc Surg. 1994 Dec;4(6):385-91. doi: 10.1089/lps.1994.4.385.
PubMed 7881141Mulier JP, Dillemans B, Van Cauwenberge S. Impact of the patient's body position on the intraabdominal workspace during laparoscopic surgery. Surg Endosc. 2010 Jun;24(6):1398-402. doi: 10.1007/s00464-009-0785-8. Epub 2010 Jan 7.
PubMed 20054583Simanski , R. Kahler, B. Pohl, R. Hofmockel, R. Friedrich, B. P. Lampe Measurement and control of neuromuscular blockade and depth of anaesthesia. Proceedings of the European Control Conference, Cambridge/UK. 2003.
Study at a glance
From the registry record, last updated by the sponsor on 28 Jul 2017. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Grading System for Laparoscopic Visualization and Predicting Factors That Affect Visualization Level During Laparoscopic Cholecystectomies: A Prospective, Single Group, Open Label Study
- ClinicalTrials.gov ID
- NCT02264444
- Acronym / sponsor ID
- 461326
- Conditions
- Cholecystitis
- Keywords
- Cholecystectomy, visualization, single incision
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 30 participants (actual)
- Lead sponsor
- Florida Hospital Tampa Bay DivisionUniversity, hospital or other
- Collaborators
- Merck Sharp & Dohme LLC
- Study start
- Sep 2013
- Primary completion
- Jun 2016 (actual)
- Study completion
- Aug 2016 (actual)
- First posted
- 15 Oct 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Essential to laparoscopic operations is adequate visualization. Unfortunately there is no grading system to assess the degree or quality of visualization. The primary objective of the project is to develop a laparoscopic visualization scoring system. We also intend to investigate the effects of neuromuscular blockade agents on visualization.
Detailed description
Essential to laparoscopic operations is adequate visualization. Unfortunately there is no grading system to assess the degree or quality of visualization. There are many contributing factors that either assist or hinder the quality. Compared to open surgical procedures, laparoscopic surgical procedures (Laparo-endoscopic Single Site (LESS) and conventional multiport) are associated with less postoperative pain, a lower wound infection rate, shorter length of hospital stays and reduced incidence of late ventral hernia(1). Despite these well documented benefits of laparoscopic procedures, laparoscopy in certain patient populations can be challenging. Preoperative factors that contribute to technical difficulty in performance of laparoscopic procedures include male gender, android body habitus, and body mass index (BMI) greater than 30 kg/m2(2). Men often have an android body habitus, whereby the excess body fat concentrates within the peritoneal cavity, increases intra-abdominal pressure and thus reduces intraoperative laparoscopic visualization. Intra-abdominal pressure measured in morbidly obese patients is 2-3 times higher than in non-obese patients. In addition, android body habitus and high BMI are often associated with an enlarged left lobe of the liver. These factors can contribute to the degree of intraoperative technical difficulty and should be weighed in selection of appropriate patients to undergo laparoscopic procedures.
Particularly in the early period of the surgeon's learning curve, we suggest that selection criteria for laparoscopic procedures for the upper abdomen be limited to patients with a low BMI and no previous upper abdominal surgery. Although low BMI is a relatively good predictor of a less challenging laparoscopic procedure, a high BMI does not necessarily predict intraoperative technical difficulty. We predict that the best method to determine the technical difficulty of laparoscopic procedures is during intraoperative evaluation. For example, the primary limiting factor in determining the technical difficulty of laparoscopic Roux-en-Y gastric bypass (RYGBP) is the size and thickness of the left lobe of the liver. A massively enlarged left lobe of the liver obscures the laparoscopic view of the gastro-esophageal junction and angle of His, making the gastrojejunal anastomosis difficult to construct. Schwartz et al. support this concept when they found that a large liver was the primary reason for conversion from laparoscopic to open RYGBP in an analysis of 1,000 patients (2).
A laparoscopic operation consists of making small punctures into the peritoneum, through which, a camera and surgical instruments are subsequently inserted. The laparoscopically placed camera is the only view of the operative field. Since this point of view is constantly changing to meet the surgeon's needs during the operation, and because it is very different from the exoscopic view of the surgeon, the surgeon has to be very well trained to interpret the images through the laparoscopic view. For LESS operations, a deflectable tip laparoscope is utilized in aiding the surgeon for improved visibility and less clashing of instruments.
The laparoscopic view does not reveal, at one time, all the structures the surgeon needs to see in order to complete the surgical procedure with success. These structures can, for instance, be hidden behind the peritoneal wall (e.g., the ureter). This limitation cannot only lead to a less efficient operation, but can also lead to complications. Often such structures can be extracted from preoperative CT/MR images; however, the surgeon needs to interpret and fuse these images with the laparoscopic view. To alleviate this problem, we propose a laparoscopic visualization scoring system based on the intraoperative quality of images (3).
The impact of muscle relaxants on the isolated abdominal wall or diaphragmatic behavior and the absolute intra-abdominal volume are difficult to measure. Conversely, the inflated volume-pressure relationship of the abdominal cavity is easier to measure. A description of this volume-pressure relationship has not been identified in previous studies. Clinical data supports a positive linear correlation between the depth of neuromuscular blockade and abdominal wall and diaphragmatic relaxation and compliance (4). There is a very tangible and real effect of the neuromuscular blockade; this ultimately has a direct impact on the quality of visualization of the surgical field during a laparoscopic procedure (5). A constant neuromuscular block leads to preferable working conditions for the surgeon. The evoked muscle responses after neurostimulation can be registered by electromyography (EMG), mechanomyography (MMG) and acceleromyography (AMG). In principle, different peripheral nerves can be used for neurostimulation. The EMG records the electrical signal generated by the muscular action potential under its surface electrodes. The force of the thumb after stimulation can be registered by MMG. The AMG records the acceleration of the thumb after neurostimulation. The EMG, MMG and AMG system allows for observation of the measured signals quantity and quality (6).
We have identified other relevant factors that significantly affect the quality of visualization during different laparoscopic procedures including:
- Clarity, focus and brightness: The laparoscope typically consists of an outer ring of optical fibers used to transmit light into the body, and an inner core of rod lenses that illuminate visual scene. This is then relayed back to the camera. Various different types of laparoscopes are available; they are specified in terms of overall length, number of rods, diameter and angle of view. Generally speaking, the wider the scope the brighter the resulting image. Lenses are available in the range of 1.9mm to 12mm, but sizes of 5mm and 10mm are the most common choices for pediatric and adult patients, respectively.
- Breadth of intra-abdominal field and vertical space measured in centimeters: Breadth of intra-abdominal field and vertical space are factors directly related to pressure insufflation as well as the level of the neuromuscular blockade.
- Distracting factors: This specific category of distracting factors includes:
- Blood: the presence, especially in large quantities, may prevent adequate visualization.
- Smoke: unipolar electrocautery and/or the bipolar Maryland forceps produce smoke when used. The rate of aspiration and evacuation also affect visualization.
- Adhesions: the presence of intra-abdominal adhesions, which hinders and prohibits proper identification of the anatomic structures.
- Sterile iodine impregnated covering sheet: its application presumably has a negative impact on abdominal wall and diaphragmatic compliance, and therefore, may obscure visualization.
- Intra-intestinal air: the presence of air inside the stomach, and small and large intestines adversely affects the size of the visual field. This can be prevented by an adequate preoperative bowel preparation and placement of an aspiration NG tube during anesthesia induction.
- Patient's specific factors such as BMI value and body habitus: From our experience, a BMI under 26 allows for optimal field visualization. Conversely, a BMI greater than 26 negatively impacts the visual field. However, a recent study conducted by Camani et al. in 2010 showed that the laparoscopic approach in the various applications of gynecologic surgery is not significantly influenced by BMI in terms of surgical outcomes, laparotomy conversion rate, intraoperative and postoperative complication rate, and duration of hospital stay (4). We feel that visualization during operations involving the abdominal cavity are adversely affected by high amounts of adipose tissue, and therefore, a visualization scoring system will help support this theory.
- Type of disorder (malignant vs. benign) that the laparoscopic procedure is undertaken for: Due to many pathologic factors such as the need for R0 resections, the discovery of more advanced disease than anticipated, the presence of adhesions or scar tissue from previous operations, laparoscopic procedures for malignant disorders may require a better visualization field than laparoscopic procedures undertaken for benign disorders.
- Inadequate and/or poorly designed instruments: Most laparoscopic instrument development is technology-driven. This approach to instrument design does not always consider the ergonomics of the users, therefore leading to a user-unfriendly product (4, 5).
- Technical difficulties: An intraoperative technical difficulty is defined as a significant deviation from the ordinary surgical procedure. All conversions to an open operation and iatrogenic bowel perforation during laparoscopic surgery are examples of technical difficulties. Many studies demonstrate that a technical difficulty during laparoscopic-assisted surgery jeopardizes both the intra-operative and postoperative patient safety.
- Patient's body position during laparoscopic procedure:
A study led by Mulier, J et al. in 2010 demonstrated that the Trendelenburg position for lower abdominal surgery and reverse Trendelenburg with flexing of the legs at the hips for upper abdominal surgery effectively improved the workspace in obese patients, even with full muscle relaxation (6).
II. Objectives A.Primary Objective The primary objective is to develop a laparoscopic visualization scoring system.
- Secondary Objectives
The secondary objectives are:
- To determine how visualization is affected by various levels of pneumoperitoneum correlated with neuromuscular blockade.
- Identify the factors that influence visualization, and determine how to manage these factors to optimize visualization.
- Determine if there is a statistically significant correlation between different degrees of visualization and the following intraoperative time intervals:
- surgical incision to sterile wound dressing
- sterile wound dressing to extubation
- sterile wound dressing to patient exiting operating room
- Determine if there is a statistically significant correlation between different degrees of visualization and postoperative pain.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Cholecystectomy visualization | Experimental | Other: Cholecystectomy visualizationAll patients will undergo a standard single site cholecystectomy and will have their operation recorded and scored for visualization. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Signed informed consent
- 18 years of age and older
- All patients deemed to have a clinical and surgical indication to undergo a LESS cholecystectomy
Key exclusion criteria (11 listed)
- Pregnancy
- Breastfeeding
- BMI>35
- Serious comorbidities precluding a LESS cholecystectomy
- Known or suspected neuromuscular disorders impairing neuromuscular function
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Cholecystectomy visualizationPatients undergo a standard removal of the gallbladder through a single incision at the umbilicus will have their operation recorded and graded according to a scale that is established for this study. | Other | Cholecystectomy visualization |
Primary outcome
Laparoscopic Visualization Score assessment
Time frame: Start to end of LESS Cholecystectomy
4 secondary outcomes
pneumoperitoneum volume
Time frame: start to end of LESS cholecystectomy
factors influencing visualization
Time frame: start to end of LESS cholecystectomy
Degrees of visualization
Time frame: start to end of LESS cholecystectomy
postoperative pain
Time frame: every day until 7 days after LESS cholecystectomy
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 28 Jul 2017.
- Background: PubMed 9479730Schrenk P, Woisetschlager R, Rieger R, Wayand WU. A diagnostic score to predict the difficulty of a laparoscopic cholecystectomy from preoperative variables. Surg Endosc. 1998 Feb;12(2):148-50. doi: 10.1007/s004649900616.
- Background: PubMed 16105411Nguyen NT, Longoria M, Gelfand DV, Sabio A, Wilson SE. Staged laparoscopic Roux-en-Y: a novel two-stage bariatric operation as an alternative in the super-obese with massively enlarged liver. Obes Surg. 2005 Aug;15(7):1077-81. doi: 10.1381/0960892054621062.
- BackgroundStijn de Buck, Johan van Cleynenbreugel, Indra Geys, Thomas Koninckx, Philippe R Koninck, Paul Suetens. A System to Support Laparoscopic Surgery by Augmented Reality Visualization. Medical Image Computing and Computer-Assisted Intervention; 691-8, 2001.
- Background: PubMed 20619751Camanni M, Bonino L, Delpiano EM, Migliaretti G, Berchialla P, Deltetto F. Laparoscopy and body mass index: feasibility and outcome in obese patients treated for gynecologic diseases. J Minim Invasive Gynecol. 2010 Sep-Oct;17(5):576-82. doi: 10.1016/j.jmig.2010.04.002. Epub 2010 Jul 8.
- Background: PubMed 7881141McDougall EM, Figenshau RS, Clayman RV, Monk TG, Smith DS. Laparoscopic pneumoperitoneum: impact of body habitus. J Laparoendosc Surg. 1994 Dec;4(6):385-91. doi: 10.1089/lps.1994.4.385.
- Background: PubMed 20054583Mulier JP, Dillemans B, Van Cauwenberge S. Impact of the patient's body position on the intraabdominal workspace during laparoscopic surgery. Surg Endosc. 2010 Jun;24(6):1398-402. doi: 10.1007/s00464-009-0785-8. Epub 2010 Jan 7.
- BackgroundSimanski , R. Kahler, B. Pohl, R. Hofmockel, R. Friedrich, B. P. Lampe Measurement and control of neuromuscular blockade and depth of anaesthesia. Proceedings of the European Control Conference, Cambridge/UK. 2003.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Alexander S. Rosemurgy, MD principal investigator
Florida Hospital Tampa Bay Division
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Cholecystectomy visualization in people with Cholecystitis, run by Florida Hospital Tampa Bay Division at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 28 Jul 2017. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Laparoscopic Visualization Score assessment (time frame: Start to end of LESS Cholecystectomy). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02264444, which also lists 7 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Jul 2017.