Clinical trials: Operation Time
Pain, Postoperative, Postoperative Pain, Acute
Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries
This is a double-arm randomized control trial evaluating the impact of preoperative opioid-free analgesia on time to trial of void in ambulatory urogynecologic surgeries.
- Trial name
- NCT06379425
- Testing
- Acetaminophen, Celecoxib, Gabapentin
- Where
- United States
- Volunteers
- 70 people, healthy volunteers welcome
- Sponsor
- Northwell Health
Anesthesia
The Effectiveness of the Addition of Dexmedetomidine to Analgesia for Ankle Surgery.
Forefoot surgeries involve a relatively short operation usually completed in 1 - 1½ hours, with patients generally being allowed to go home on the same day.
- Trial name
- NCT02170948
- Testing
- Dexmedetomidine
- Where
- Canada
- Volunteers
- 12 people
- Sponsor
- University Health Network, Toronto
Cataract
Manipulating Temporal Expectations to Accelerate Recovery After Cataract Surgery
This study tested whether changing how quickly patients expect to heal after cataract surgery changes how quickly their vision recovers. Adults having cataract surgery in both eyes were randomly assigned to one of two groups.
- Trial name
- NCT07899112
- Testing
- Faster-timeline video and healing-attention surveys, Standard-timeline video and matched surveys
- Where
- 2 sites in United States
- Volunteers
- 147 people
- Sponsor
- Harvard University
Infection Secondary to Surgical Procedure
Effect of Chlorhexidine Gluconate Hair Bath on the Development of Surgical Site Infection and Time to Discharge
One of the most important preventable complications occurring in the postoperative period is surgical site infections. Surgical site infections (SSI) are infections that occur in incisions, organs or organ spaces that occur after…
- Trial name
- NCT06763211
- Testing
- Chlorhexidine Hair Bath
- Where
- Turkey (Türkiye)
- Volunteers
- 84 people
- Sponsor
- HAVVA ÇOŞKUN
Hip Arthroplasty
Stem Cells Predicting Orthopedic Outcomes
This is a pilot study to provide preliminary data of the association between bone mineral denity adjacent to acetabular implants, as measured by quanitative computed tomography (QCT), at least 2 years post Total Hip Arthoplasty…
- Trial name
- NCT01366911
- Where
- United States
- Volunteers
- 203 people, healthy volunteers welcome
- Sponsor
- University of Nebraska
Forearm Injuries, Radius Fractures
Time to Healing in Displaced Pediatric Diaphyseal Forearm Fractures Treated With Bioabsorbable Compared to Titanium Intramedullary Nails
This study looks at children with forearm fractures that need surgery. The standard treatment uses titanium nails, which usually need to be removed in a second operation later.
- Conditions
- Forearm Injuries, Radius Fractures, Ulna Fractures, Fractures, Bone
- Trial name
- FOREST (NCT07536581)
- Testing
- Bioabsorbable intramedullary nail, Titanium elastic intramedullary nail
- Where
- Denmark
- Volunteers
- 60 people
- Sponsor
- Children's Fractures Interest Group, Denmark
Fluid Overload, Organ Edema
"The Effect of Reduced Fluid Load After Cardiac Surgery"
The purpose of this study is to verify that an infusion of hypertonic saline/colloids during cardio-pulmonary-bypass will reduce fluid overload and organ edema for cardiac patients with expected long-CPB-time.
- Conditions
- Fluid Overload, Organ Edema, Organ Function
- Trial name
- NCT01438502
- Testing
- HyperHAES® (hypertonic saline/HES)
- Sponsor
- Haukeland University Hospital
Early Career Surgeons, Mental Wellbeing
The MICROSCOPE Project
This multicenter observational prospective study aims to explore the impact of peri-operative support measures (mentorship or coaching or intraoperative consultation) on the mental well-being of early career surgeons.
- Conditions
- Early Career Surgeons, Mental Wellbeing, Patients Outcomes, Mentorship
- Trial name
- MICROSCOPE (NCT07153224)
- Testing
- Peri-operative support measures [mentorship, intraoperative consult, surgical coaching, standard practice (no structured support)]
- Where
- Italy
- Volunteers
- 340 people
- Sponsor
- Niguarda Hospital
Hemodynamic Instability
Hemodynamic Optimization During Major Urological Surgery
In this prospective observational study investigators aim to seek for any possible correlation between the venous to arterial carbon dioxide difference (pCO2 gap) at the end of surgery and the percentage of time spent above a…
- Trial name
- INTAT (NCT03474224)
- Testing
- Ev1000 Clinical Platform from Edwards Lifesciences
- Where
- Italy
- Volunteers
- 30 people
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Thoraric Surgery, Surgery Time Expected More Than Two Hours
Individualized Perioperative Open-Lung Ventilatory Strategy During One-Lung Ventilation
The purpose of this study is to determine whether individualized ventilatory management during one-lung ventilation in patients scheduled for thoracic surgery, combining the use of low tidal volumes, alveolar recruitment…
- Trial name
- iPROVE-OLV (NCT03182062)
- Testing
- Alveolar recruitment maneuver, PEEP Titration Trial, Lung protective ventilation
- Where
- 4 sites in Spain
- Volunteers
- 1,400 people
- Sponsor
- Fundación para la Investigación del Hospital Clínico de Valencia
Referral and Consultation, Telemedicine
Electronic Referral and Booking of Outpatient Day Case Surgery Compared With Traditional Referral Routines.
We want in this study to investigate the cost-effectiveness and waiting time of direct electronic referral and booking of outpatient surgery compared to the traditional patient pathway where the patient is seen at the outpatient…
- Conditions
- Referral and Consultation, Telemedicine, Surgery, Outpatient, Surgery, Day
- Trial name
- one-stop (NCT00692497)
- Testing
- one stop (Electronic standardised referrals and appointment bookings)
- Where
- Norway
- Volunteers
- 120 people
- Sponsor
- University Hospital of North Norway
Stress Urinary Incontinence
Does Bladder Instillation Reduce Time to Discharge After Sling Surgery
The purpose of this randomized control trial study is to determine if intraoperative bladder instillation of fluid decreases the time to discharge after having an outpatient mid-urethral sling procedure, and to measure the cost…
- Trial name
- NCT02277288
- Testing
- Filled bladder arm
- Where
- United States
- Volunteers
- 250 people
- Sponsor
- Cedars-Sinai Medical Center
Arthroplasty, Replacement, Hip
Visibility of Site Marking for Surgical Time Out With Two Different Skin Preparation Solutions
Skin preparation solutions are used to clean the skin of the patient before surgery to decrease the rate of infection. This is particularly important for hip replacement to reduce the risk of prosthetic joint infection.
- Trial name
- site marking (NCT00739583)
- Testing
- CHG 2% w/v and IPA 70% v/v, Iodophor 0.7% and IPA 74% w/w
- Where
- United States
- Volunteers
- 20 people
- Sponsor
- Johns Hopkins University
Skull Base
Bed Rest Duration and Outcomes in Endoscopic Skull Base Reconstruction
This study is a randomized controlled trial conducted across multiple centers. Due to the anatomical and pathological complexity of endoscopic endonasal skull base surgery, the study scope was restricted to the midline anterior…
- Trial name
- BRO (NCT07465861)
- Testing
- non-bed-rest, 2-day bed-rest, 1-day bed-rest
- Volunteers
- 316 people
- Sponsor
- The Affiliated Hospital of Qingdao University
First-attempt Success Rate of Real-time Ultrasound-guided Thoracic Epidural Catheter Placement
Application of Real-time Ultrasound Guidance in Thoracic Epidural Catheter Placement
The goal of this clinical trial is to assess the success rate of real-time ultrasound-guided thoracic epidural catheter placement at the first attempt in patients who will undergo thoracic or abdominal surgeries.
- Trial name
- NCT07100769
- Testing
- Real-time ultrasound-guided thoracic epidural placement
- Where
- Vietnam
- Volunteers
- 100 people
- Sponsor
- University Medical Center Ho Chi Minh City (UMC)
Coronary Artery Disease
Residents' Learning Curve of Intraoperative Transit-time Flowmetry and High-frequency Ultrasound in CABG (LEARNERS)
Transit-time flowmetry (TTFM) allows grafts quality assessment during coronary artery bypass surgery by measuring the flow volume through them.
- Trial name
- LEARNERS (NCT06589323)
- Testing
- Coronary artery bypass graft
- Where
- Italy
- Volunteers
- 80 people
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Breast Cancer, Surgery
Study to Assess the Impact of Personalized Coaching on the Time Period and Quality of Return to Work After Breast Cancer
Evaluate the impact of coaching sessions on the return to work rate (number of patients returning at work / total number of patients per arm) 6 months after inclusion in the study for breast cancer in professionnally active…
- Trial name
- OPTICOACH (NCT04469205)
- Testing
- Coaching sessions
- Where
- 2 sites in France
- Volunteers
- 69 people
- Sponsor
- Institut Curie
Gastrectomy, Obesity
Endoscopic vs. Suction Device Calibration in Sleeve Gastrectomy
This study aims to compare the difference in staple usage and post-operative GERD (heartburn) between patients that had an endoscope used versus patients that had a suction calibration system used on them during "laparoscopic…
- Trial name
- NCT03939819
- Testing
- ViSiGi® 3D suction calibration device, Esophagogastroduodenoscopy (EGD) calibration
- Where
- United States
- Volunteers
- 106 people
- Sponsor
- Emory University
Analgesia, Caffeine
Caffeine Intake Inrelation to Perioperative Analgesic Consumption
Caffeine is the most widely consumed psychoactive drug in the world. Natural sources of caffeine include coffee, tea, and chocolate.
- Trial name
- NCT05330754
- Testing
- Caffeine intake in mg
- Where
- Egypt
- Volunteers
- 90 people
- Sponsor
- Ain Shams University
Pulmonary Air Leak
Effects of Local Protocols on Duration of Chest Tube Therapy Following Thoracic Surgery
The effect of local chest-tube management protocols on the duration of chest-tube therapy following thoracic surgery was analyzed in four German specialized Thoracic Surgery Units.
- Trial name
- NCT01467622
- Testing
- Chest tube removal
- Where
- 4 sites in Germany
- Volunteers
- 80 people
- Sponsor
- Schillerhoehe Hospital