Clinical trials: Elective Surgeries
Peripheral Perfusion, Bowel Ischemia
Peripheral and Mesenteric Perfusion in Elective Surgical Patients
An important goal of haemodynamic monitoring and resuscitation is early detection of insufficient tissue perfusion and oxygenation.
- Conditions
- Peripheral Perfusion, Bowel Ischemia, Colorectal Surgery, Haemodynamic Instability
- Trial name
- NCT03395483
- Testing
- Haemodynamic monitoring
- Where
- Denmark
- Volunteers
- 30 people
- Sponsor
- Hvidovre University Hospital
Venous Thromboembolism
Dose-confirmatory Bridging Study in Total Hip Replacement
The objective of this dose-confirmatory bridging study is to investigate the safety and efficacy of rivaroxaban 5 to 10 mg once-daily (od) dosing in the prevention of venous thromboembolism (VTE) in Japanese patients undergoing…
- Trial name
- NCT01205932
- Testing
- Rivaroxaban (BAY59-7939), Enoxaparin
- Where
- 41 sites in Japan
- Volunteers
- 402 people
- Sponsor
- Bayer
Postoperative Quality of Recovery, Postoperative Migrainous Headache
Effect of Sumatriptan on the Postoperative Quality of Recovery After Elective Minimally Invasive Craniotomy
Postoperative migrainous headache following craniotomy is distressing and may cause significant morbidity and often delay discharge from the hospital. The mechanism of this post craniotomy migraine is multifactorial.
- Trial name
- NCT01632657
- Testing
- Sumatriptan
- Where
- Canada
- Volunteers
- 40 people
- Sponsor
- University Health Network, Toronto
Hemodynamic Instability
Impact of Fluid Management Within a Goal-directed Hemodynamic Protocol on Acid-base Balance in Elective Trauma Surgery
The purpose of this study is to determine whether the administration of a compound of balanced infusion solutions including 50% crystalloid and 50% colloid has a positive impact on acid-base balance in elective hip replacement…
- Trial name
- HIPSTER (NCT01117519)
- Testing
- Infusion Therapy
- Where
- Germany
- Volunteers
- 40 people
- Sponsor
- Charite University, Berlin, Germany
Gastrointestinal Complication
Evaluation of the PrevisEA Device for Predicting Gastrointestinal Impairment
PrevisEA is a noninvasive, disposable device that uses audio spectral analysis of sounds produced by the gastrointestinal tract to predict gastrointestinal impairment (GII).
- Trial name
- NCT04880473
- Testing
- PrevisEA device
- Where
- 8 sites in United States
- Volunteers
- 400 people
- Sponsor
- Entac Medical Inc.
Postoperative Complications
Predictors of 30-day Postoperative Outcome After Elective EVAR
This study investigated the 30-day postoperative outcome after elective EVAR and the role of possible predictors among patients' baseline characteristics
- Trial name
- NCT05647486
- Testing
- 30-day postoperative outcome
- Where
- Greece
- Volunteers
- 322 people
- Sponsor
- University of Thessaly
Elective Fertility Preservation
Study of the Prevalence of Endometriosis and Adenomyosis
Our study aims to assess the prevalence of adenomyosis and endometriosis in patients consulting for elective fertility preservation through the diagnosis of these pathologies by transvaginal pelvic ultrasound.
- Trial name
- PrevADEOSE (NCT06211569)
- Testing
- Usual follow-up
- Where
- France
- Volunteers
- 400 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Coronary Artery Disease (CAD), Left Ventricular (LV) Systolic Dysfunction
Ketamine-lidocaine Versus Ketamine-fentanyl for Induction of Anesthesia in Patients With Left Ventricular Systolic Dysfunction Undergoing Elective Coronary Artery Bypass
This study compares ketamine/fentanyl versus ketamine/lidocaine in term of their impact on cerebral perfusion during CABG. No prior data address these effects, and the goal is to identify the induction regimen that better…
- Conditions
- Coronary Artery Disease (CAD), Left Ventricular (LV) Systolic Dysfunction, Induction Anesthesia, Coronary Bypass Graft Surgery
- Trial name
- NCT07248202
- Testing
- Fentanyl (IV), lidocaine
- Where
- Egypt
- Volunteers
- 48 people
- Sponsor
- Cairo University
Delayed Cord Clamping
Umbilical Cord Clamping: What Are the Benefits
Umbilical cord clumping consists in the binding of the umbilical cord by nipper to interrupt blood flow from placenta to foetus. Umbilical cord can be clamped within 30s or at least 1 min after birth.
- Trial name
- NCT03878602
- Testing
- Delayed umbilical cord clamping, Immediate umbilical cord clamping
- Where
- Italy
- Volunteers
- 142 people
- Sponsor
- Fondazione Poliambulanza Istituto Ospedaliero
Postoperative Pain Status of Patients Who Underwent Elective Laparoscopic Cholecystectomy
Are Neutrophil-Lymphocyte Ratio, Platelet-Lymphocyte Ratio, and Systemic Immune Inflammation Score Values Indicators for Postoperative Pain?
Postoperative pain status of patients who underwent elective laparoscopic cholecystectomy.
- Trial name
- NCT05558553
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 2 people
- Sponsor
- Samsun University
Abdominoplasty, Perioperative Analgesia
Combined Ultrasound Guided Bilateral Rectus Sheath and Erector Spinae Plain Blocks Versus Erector Spinae Plain Block for Intra and Postoperative Analgesia in Elective Abdominoplastic Surgeries. a Randomized Controlled Double Blinded Trial.
The goal of this clinical trail is to determine if bilateral erector spinae plane block alone can provide good perioperative analgesia for abdominoplastic surgery patients or it is better to give combined bilateral rectus sheath…
- Trial name
- NCT06765772
- Testing
- Erector spinae plane block, Rectus sheath block
- Where
- Egypt
- Volunteers
- 40 people
- Sponsor
- Cairo University
Regional Anesthesia, Caeserian Section
Continuous Infusion for Pain Relief
SPINAL anesthesia is commonly used for cesarean section, and it has become a popular practice to add opioids to spinal solutions to enhance and prolong intraoperative and postoperative analgesia.
- Conditions
- Regional Anesthesia, Caeserian Section, Local Anesthetic
- Trial name
- NCT02711072
- Testing
- control group, infiltration group
- Volunteers
- 60 people
- Sponsor
- Tunisian Military Hospital
Colorectal Cancer, Inflammatory Bowel Diseases
Home To Stay: a Randomized Trial Evaluating a Post-discharge Mobile App for Elective Colorectal Surgery
A single center randomized controlled trial to evaluate the effect of a post-discharge mobile health application on 30-day re-admission and patient reported outcomes following elective colorectal surgery
- Conditions
- Colorectal Cancer, Inflammatory Bowel Diseases, Utilization, Health Care, Surgery
- Trial name
- NCT04968145
- Testing
- Home To Stay Mobile Health Application
- Where
- Canada
- Volunteers
- 282 people
- Sponsor
- Division of General Surgery , Mt. Sinai Hospital
Hemodynamic Stability
Comparative Analytical Study of Intravenous Bolus Dose of Mephentermine and Phenylephrine for Hemodynamic Stability During Elective Cesarean Section Under Spinal Anesthesia at KIST Medical College and Teaching Hospital
Hemodynamics changes with spinal anesthesia is mainly due to sympathetic block which causes mainly hypotension \& bradycardia. Post spinal hypotension usually leads to various adverse maternal and fetal outcomes.
- Trial name
- NCT05706727
- Testing
- Intravenous bolus dose of Mephentermine and mephentermine, intravenous bolus dose of phenylephrine 50 mcg
- Where
- Nepal
- Volunteers
- 42 people, healthy volunteers welcome
- Sponsor
- KIST Medical and Teaching Hospital
Pregnancy
Changes in Ventilation Inhomogeneity and Respiratory Function Following Elective Caesarean Section Under Regional Anaesthesia
Pregnancy is associated with physiological changes affecting the cardiorespiratory system as a consequence of an increase in both cardiac output and intra-abdominal pressure.
- Trial name
- VIRCA (NCT02714556)
- Testing
- Physiologic measures of lung function
- Where
- Switzerland
- Sponsor
- Walid HABRE
Obstetrics: Elective Caesarean Delivery
Effects of Spinal Anesthesia on the Fetal Autonomic Nervous System
Elective cesarean deliveries account for over 10% of births in France and are often scheduled around 39 weeks of gestation. When feasible, spinal anesthesia is considered the gold standard in such a clinical situation.
- Trial name
- RACHISNA (NCT07333729)
- Testing
- Recording of fetal and maternal heart rate
- Where
- France
- Volunteers
- 50 people
- Sponsor
- University Hospital, Lille
Airway Management, Tracheal Intubation
Comparison of Intubation Using Video Laryngeal Mask and Video Laryngoscope in Elective Surgical Patients
This study compares two airway devices that are commonly used during elective surgery: the video laryngeal mask airway (VLM) and the video laryngoscope (VLS). Both are part of routine anesthesia practice.
- Conditions
- Airway Management, Tracheal Intubation, Elective Surgeries, Videolaryngoscopy
- Trial name
- NCT07057908
- Testing
- Video Laryngoscope Intubation with Bougie, Video Laryngeal Mask Airway (SaCoVLM) Intubation with Bougie
- Where
- Turkey (Türkiye)
- Volunteers
- 176 people
- Sponsor
- Samsun University
Cesarean Section
Parents' Expectations and Experiences Around Cesarean Section in Belgium
The aim of this study is to gain insight in the experiences and expectations of Belgian parents concerning primary cesarean section.
- Trial name
- NCT02609217
- Testing
- Questionnaires and interviews
- Where
- Belgium
- Volunteers
- 24 people
- Sponsor
- Universitaire Ziekenhuizen KU Leuven
Portosystemic Shunt
To Compare the Outcome of Temporary Portocaval Shunt During Recipient Hepatectomy Versus No Shunt in Adult Elective Live Donor Liver Transplantation.
Temporary portocaval Shunt during recipient hepatectomy improves intra operative parameters and morbidity in LDLT recipients
- Trial name
- NCT05385120
- Testing
- Temporary Portocaval Shunt
- Volunteers
- 40 people
- Sponsor
- Institute of Liver and Biliary Sciences, India
Smoking
Pilot Study: Preoperative Nicotine Lozenges
The goal of this pilot study is to determine the feasibility and potential effect size of nicotine lozenges as an adjunct to maintain brief preoperative abstinence, defined as not smoking the day of surgery.
- Trial name
- NCT00586482
- Testing
- Nicotine Lozenge, Abstinence Advisement
- Where
- United States
- Volunteers
- 46 people
- Sponsor
- Mayo Clinic
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