Clinical trials: Surgical Procedure, Unspecified
Anesthesia, Surgical Procedure, Unspecified
Ultrasound Assessment of Gastric Content for Semi Emergency Surgery
Aspiration of gastric content is a rare but serious complication of anesthesia. In this context, preoperative fasting for elective surgery is well defined.
- Trial name
- ECHO-GAST (NCT02386787)
- Testing
- Ultrasonography
- Where
- France
- Volunteers
- 300 people
- Sponsor
- Centre Hospitalier Universitaire de Saint Etienne
Pain, Acute, Surgical Procedure, Unspecified
Surgical Intervention in Deep Sedation: No Pain or no Memory
The goal of this observational study is to assess the levels of nociception in deeply sedated patients who need painful and short-duration surgical procedure.
- Trial name
- SedNOL (NCT06963749)
- Where
- Italy
- Volunteers
- 36 people, healthy volunteers welcome
- Sponsor
- ASL Novara
Infant Apnea, Surgical Procedure, Unspecified
Apneic Oxygénation by Nasal Canula During Infants Airway Management Study
This is a randomized clinical trial investigating the utility of apneic oxygenation via high flow nasal cannulae during airway management for infants general anaesthesia.
- Conditions
- Infant Apnea, Surgical Procedure, Unspecified, Airway Management
- Trial name
- Oxyeno (NCT03967769)
- Testing
- High Flow nasal Cannula
- Where
- France
- Volunteers
- 72 people
- Sponsor
- University Hospital, Clermont-Ferrand
Surgical Procedure, Unspecified
New Use of the ViKY Device for Uterus Positioning
Evaluation of Safety and Efficacy of ViKY Device for Uterus Positioning on 2 US sites
- Trial name
- NCT01531504
- Testing
- ViKY UP
- Where
- 2 sites in United States
- Volunteers
- 30 people
- Sponsor
- EndoControl
Isthmic Spondylolisthesis, Surgical Procedure, Unspecified
Isthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes
This study aims to evaluate clinical and radiological outcomes of isthmic spondylolisthesis surgically treated with combined approach.
- Trial name
- SPLAC (NCT03585439)
- Testing
- Observational study evaluating the results of an intervention for isthmic spondylolisthesis: surgical procedure with double approach: Anterior lumbar Interbody Fusion then postero-lateral fusion
- Where
- France
- Volunteers
- 87 people
- Sponsor
- CMC Ambroise Paré
Gynecologic Cancer, Surgical Procedure, Unspecified
Laparoscopic Ultrasound Examination: Analysis of Feasibility
This is a prospective cohort study to assess the feasibility of the laparoscopic ultrasound examination, directly by surgeons, during minimally invasive gynaecological surgery.
- Trial name
- LUXA (NCT06278636)
- Testing
- Laparoscopi ultrasound examination
- Where
- Italy
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Nociceptive Pain, Surgical Procedure, Unspecified
Monitoring Analgesia by ANI (Analgesia The Nociception Index)
The objective of this research is to study the variations of the ANI(Analgesia The Nociception Index) according to 2 periods: the "NoStim" period before surgical incision under general anesthesia and the period of hemodynamic…
- Trial name
- ANI-MICI (NCT03749304)
- Testing
- ANI monitor
- Where
- France
- Volunteers
- 25 people
- Sponsor
- University Hospital, Lille
Other Reconstructive Surgery, Failure of Muscle Graft
Robotic Harvest of the Latissimus Dorsi (LD) Muscles
The goal of this clinical research study is to learn more about the safety and feasibility of using the Da Vinci Robotic Surgical system in procedures that harvest the latissimus dorsi muscle (a back muscle below your shoulder)…
- Conditions
- Other Reconstructive Surgery, Failure of Muscle Graft, Cancer, Complications
- Trial name
- NCT02274493
- Testing
- da Vinci® Robotic Surgical System, LD muscle flap harvest procedure, Reconstructive surgery
- Where
- United States
- Volunteers
- 15 people
- Sponsor
- M.D. Anderson Cancer Center
Lumbar Disc Disease, Surgical Procedure, Unspecified
Evaluation of the Contribution of Intraoperative Scans Coupled With the Navigation for the Precision of the Positioning of the Pedicle Screws During a Lumbar Spine Surgery: a Prospective Randomised Study
Investigators team propose to evaluate the impact of the use of intraoperative scanning coupled with Stryker navigation, compared to the conventional fluoroscopy technique, on the accuracy of pedicle screws, in instrumented…
- Trial name
- SCANRACH (NCT04134975)
- Testing
- Spine surgery
- Where
- France
- Volunteers
- 126 people
- Sponsor
- GCS Ramsay Santé pour l'Enseignement et la Recherche
Minimally Invasive Surgical Procedures, Abnormal Uterine Bleeding, Unspecified
Cyclobenzaprine for Postoperative Pain in Minimally Invasive Hysterectomy
Typical postoperative pain control after minimally invasive hysterectomy includes ibuprofen, acetaminophen, and a short course of narcotics.
- Conditions
- Minimally Invasive Surgical Procedures, Abnormal Uterine Bleeding, Unspecified, Adenomyosis of Uterus, Fibroid Uterus
- Trial name
- NCT07664956
- Testing
- Cyclobenzaprine
- Where
- United States
- Volunteers
- 36 people
- Sponsor
- Christiana Care Health Services
Surgery, Surgical Injury
Mini-invasive Approaches to Aortic Surgery
There are many different types of mini-invasive approaches to aortic surgery. Ministernotomy and anterior right minithoracotomy are the two main techniques applied for minimally invasive aortic valve replacement, but if one of…
- Conditions
- Surgery, Surgical Injury, Surgical Procedure, Unspecified, Surgical Incision
- Trial name
- MSvsMT (NCT04350697)
- Testing
- Aortic Surgery
- Where
- Italy
- Volunteers
- 2,425 people
- Sponsor
- University of Florence
Surgical Procedure, Unspecified
Thoracic Epidural Versus General Anaesthesia in Cholecystectomy
CONTEXT AND AIMS: The aim of the study is to compare patients satisfaction of thoracic epidural and general anesthesia procedures in patients undergoing elective laparoscopic cholecystectomy.
- Trial name
- EVGAC (NCT03107832)
- Testing
- thoracic epidural anesthesia procedure
- Where
- Turkey (Türkiye)
- Volunteers
- 40 people
- Sponsor
- Abant Izzet Baysal University
Surgical Procedure, Unspecified, Postoperative Complications
Predictors, Risk Factors and Outcome Following Major Surgery
This is a multicentre, prospective, observational cohort study. Consecutive patients, operated in six University Hospitals in Sweden will be recruited following major surgical procedure.
- Trial name
- PROFS (NCT02626546)
- Testing
- Major surgical procedure
- Where
- Sweden
- Volunteers
- 1,061 people
- Sponsor
- Karolinska Institutet
Surgical Procedure, Unspecified
Development and Pilot Test of an Elective Bilateral Salpingo-Oophorectomy (BSO) Decision Support Guide
The investigators propose to conduct formative research to gain an understanding of patients' needs and desires regarding elective Bilateral Salpingo-Oophorectomy (BSO) decision making, and to develop and pilot test a BSO…
- Trial name
- BSO (NCT01369654)
- Testing
- Computerized decision aid with 1 type of value clarification
- Where
- United States
- Volunteers
- 63 people, healthy volunteers welcome
- Sponsor
- University of California, San Francisco
Quality of Life, Surgical Procedure, Unspecified
Assessing Change in Patient-reported Quality of Life After Elective Surgery: an Observational Comparison Study
This study will compare two commonly-used methods for assessing patient-reported quality of life. The first is to assess quality of life before surgery and again after surgery using the same validated scale (ie Veterans Rand 12).
- Trial name
- NCT02771964
- Testing
- Quality of life survey
- Where
- United States
- Volunteers
- 17,850 people
- Sponsor
- Washington University School of Medicine
Malignant Neoplasm, Surgical Procedure, Unspecified
Use of a Pre-Surgical Toolkit in Improving Surgical Care and Outcomes in Older Participants With Cancer
This trial studies how well the use of a pre-surgical toolkit (OPTI-Surg) works in improving surgical care and outcomes in older participants with cancer.
- Conditions
- Malignant Neoplasm, Surgical Procedure, Unspecified, Health Care Provider, Carcinoma
- Trial name
- NCT03857620
- Testing
- Best Practice, Informational Intervention, Questionnaire Administration
- Where
- 44 sites in United States
- Volunteers
- 325 people
- Sponsor
- Alliance for Clinical Trials in Oncology
Surgical Procedure, Unspecified, Anesthesia
Preoperative Anesthesia Automatic System:a Retrospective Cohort Study
To evaluate of PACMAN triage system is able to discern patient who may be safely screened by phone
- Conditions
- Surgical Procedure, Unspecified, Anesthesia, Assessment
- Trial name
- PACMAN (NCT06148701)
- Where
- Netherlands
- Volunteers
- 1,019 people
- Sponsor
- Jeroen Bosch Ziekenhuis
Surgical Procedure, Unspecified
Non-invasive Assessment of Arterial Blood Pressure and Functional Hemodynamic Parameters
Cardiac output can be monitored using different invasive devices. Nexfin HD is a new, noninvasive device that uses model flow technology to measure stroke volume and thus computes cardiac output (CO).
- Trial name
- NCT01292759
- Where
- Germany
- Volunteers
- 24 people
- Sponsor
- Johannes Gutenberg University Mainz
Surgical Procedure, Unspecified, Analgesia
Evaluation of Immersive Audiovisual Distraction Impact on Peroperative Opioid Consumption.
This study evaluate the impact of an audiovisual distraction device on the peroperative opioid consumption for outpatient procedures with Remifentanil added to local anesthesia.
- Conditions
- Surgical Procedure, Unspecified, Analgesia, Outpatient
- Trial name
- AmbuCineView (NCT04238572)
- Testing
- Audiovisual distraction device, Analgesia nociception index
- Where
- France
- Volunteers
- 200 people
- Sponsor
- University Hospital, Caen
Vertebral Osteomyelitis, Spondylodiscitis
Conservative Versus Surgical Treatment of Native Vertebral Osteomyelitis
The optimal treatment of uncomplicated native vertebral osteomyelitis (NVO) is unknown. While some authors recommend surgical treatment (consisting of spinal debridement, decompression and instrumentation using hardware…
- Conditions
- Vertebral Osteomyelitis, Spondylodiscitis, Surgical Procedure, Unspecified
- Trial name
- NCT04436328
- Testing
- Surgical treatment, Antimicrobial treatment
- Where
- Germany
- Volunteers
- 300 people
- Sponsor
- Charite University, Berlin, Germany