Clinical trials: Elective
Coronary Artery Disease
Stavanger UncomPlicatEd Elective PCI Same DaY Discharge Study (SPEEDY Study)
The purpose of this study is to provide information on safety of same day discharge after uncomplicated percutaneous intervention (PCI) for stable angina pectoris in Norwegian clinical practice.
- Trial name
- SPEEDY (NCT02513108)
- Testing
- same day discharge
- Where
- Norway
- Volunteers
- 82 people
- Sponsor
- Helse Stavanger HF
Postoperative Pain After Cesarean Section
Comparison of Combined Spinal Epidural Analgesia and Erector Spinae Plane Block After Elective Cesarean Section
Postoperative pain after cesarean section can significantly affect maternal recovery, early mobilization, and patient satisfaction.
- Trial name
- CSEA-ESP-CS (NCT07411521)
- Testing
- Combined Spinal Epidural Analgesia, Ultrasound-Guided Erector Spinae Plane Block
- Where
- Turkey (Türkiye)
- Volunteers
- 90 people
- Sponsor
- Bursa City Hospital
Airway Ultrasound Indices, Clinical Airway Assessment
Airway Ultrasound Indices for Prediction of Difficult Laryngoscopy in Pediatric Patients
The goal of this observational study is to compare the airway ultrasound indices and the preoperative clinical airway assessment concerning the difficult laryngoscopic view in paediatric patients undergoing elective surgery under…
- Trial name
- NCT07185516
- Testing
- Airway ultrasound indices, Clinical airway assessment
- Where
- Egypt
- Volunteers
- 130 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Anxiety, Pregnancy
Virtual Reality in Elective Caesarean Births Study (VREC)
This study will establish the safety of a known intervention in a novel setting. It will assess how maternal anxiety during the peri-operative period of an elective cesarean section (eCS) is affected by the introduction of a…
- Conditions
- Anxiety, Pregnancy, Pain
- Trial name
- VREC (NCT07130084)
- Testing
- Virtual Reality Educational Film
- Where
- United Kingdom
- Volunteers
- 40 people
- Sponsor
- Royal United Hospitals Bath NHS Foundation Trust
Intensive Care, Surgical
Postoperative Delirium in Adult Patients After Elective Craniotomy Under General Anaesthesia
Postoperative delirium may result in many adverse complications. At present little is known about postoperative delirium in patients after crniotomy because they may manifest similar symptoms to definitely delirium for some…
- Conditions
- Intensive Care, Surgical, Postoperative Care, Neurosurgery
- Trial name
- NCT03087838
- Where
- China
- Volunteers
- 800 people
- Sponsor
- Capital Medical University
Diagnostic Colonoscopy Screening
Remifentanil Only vs. Midazolam and Meperidine During Elective Colonoscopy
The aim of the present study is to compare patient's recovery times after elective colonoscopy employing remifentanil only vs conventional combination of midazolam and meperidine
- Trial name
- remifentanil (NCT01693185)
- Testing
- Remifentanil, Midazolam, Meperidine
- Where
- South Korea
- Volunteers
- 60 people
- Sponsor
- Konkuk University Medical Center
COVID-19, Coronavirus
Outcomes of Elective Cancer Surgery During the COVID-19 Pandemic Crisis
CovidSurg-Cancer is an international, multicentre, observational cohort study designed to evaluate the 30-day COVID-19 infection rates in elective cancer surgery during the COVID-19 pandemic.
- Conditions
- COVID-19, Coronavirus, Cancer, Surgery
- Trial name
- CovidSurg-Can (NCT04384926)
- Testing
- Elective Cancer Surgery
- Where
- Spain
- Volunteers
- 1,000 people
- Sponsor
- University of Birmingham
Elective Laparoscopic Surgery
Compare Pharmaceutical Economics and Efficacy of Sevoflurane With Low Fresh Gas Flow Balanced Anesthesia, Propofol Target Controlled Infusion Anesthesia and Propofol Induction Sevoflurane Maintenance Anesthesia
This study is being performed to compare the cost of anesthetic techniques with sevoflurane (low fresh gas flow balanced anesthesia) versus propofol (target controlled infusion [TCI]) versus propofol induction and sevoflurane…
- Trial name
- NCT01191476
- Testing
- Sevoflurane Inhalational Induction and Maintenance, Propofol Target Controlled Infusion for Induction and Maintenance, Propofol Target Controlled Infusion for Induction and Sevoflurane Inhalation for Maintenance
- Where
- 4 sites in China
- Volunteers
- 336 people
- Sponsor
- Abbott
Venous Thromboembolism
Pharmacokinetic (PK) Assessment of BIBR 1048 in Patients After Primary Elective Total Hip Replacement Surgery
To determine the PK profile of a single dose 150 mg BIBR 1048, oral capsule, administered 1-3 hours post surgery in hip replacement patients.
- Trial name
- NCT02170935
- Testing
- BIBR 1048 capsule
- Volunteers
- 62 people
- Sponsor
- Boehringer Ingelheim
Surgery
Ultrasound-guided Thoracic Paravertebral Block Using Ropivacaine With/Without Dexamethasone in Elective Thoracotomy
The procedures of thoracotomy are among the most painful operations. In addition to post-thoracotomy pain, the outcomes of surgery are affected adversely by postoperative discomfort.
- Trial name
- NCT02871193
- Testing
- Ropivacaine, Dexamethasone, saline
- Where
- China
- Volunteers
- 68 people
- Sponsor
- The First Affiliated Hospital of Anhui Medical University
Difficult / Failed Intubation
NC/TMD Ratio As a Difficult Airway Predictor in Obese Patients
To assess accuracy of NC/TM distance ratio in terms of sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV) for predicting difficult intubation in obese patient with Intubation difficulty…
- Trial name
- NCT05735106
- Where
- Pakistan
- Volunteers
- 220 people, healthy volunteers welcome
- Sponsor
- KRL Hospital, Islamabad
Urgent Caesarian Section Secondary to Cord Prolapse
Complications: Urgent C Section VS Elective C Section
The medical literature does not provide sufficient information or recommendation regarding specific antibiotic coverage for urgent Caesarian sections.
- Trial name
- NCT01524107
- Where
- Israel
- Volunteers
- 240 people
- Sponsor
- Hadassah Medical Organization
Head and Neck Cancer
Invert-Prospective Phase II Randomized Trial of Involved Nodal Versus Elective Neck RadioTherapy
To determine the risk of solitary elective volume recurrence following involved nodal radiotherapy (INRT) versus elective nodal irradiation (ENI)
- Trial name
- NCT06477692
- Testing
- ENI using IMRT with or without chemotherapy, INRT, ENI
- Where
- United States
- Volunteers
- 80 people
- Sponsor
- University of Texas Southwestern Medical Center
Asa 1 and 2 Patients for Elective Surgery Requiring Caudal as Part of Their Care
The Effect of Caudal Volumes on the Anatomical Spread of Caudals in Children
Radiological study into the anatomical spread of caudal local anaesthetic in children age 1-7
- Trial name
- NCT00232921
- Testing
- caudal volume 1, caudal volume 2, caudal volume 3
- Where
- United Kingdom
- Sponsor
- Institute of Child Health
GIT Function, Cholecystectomy, Laparoscopic
Dexamethasone, Dexmedetomidine and Their Combination on Post op. GIT Function Measured by I-FFED Score Post Laparoscopic Cholecystectomy
The goal of this clinical trial is to learn the effect of Dexamethasone and Dexmedetomidine and Their Combination on Post op. GIT Function Measured by I-FFED Score Post Laparoscopic Cholecystectomy What medical problems do…
- Conditions
- GIT Function, Cholecystectomy, Laparoscopic, Dexamethasone, Dexmedetomidine
- Trial name
- vomiting (NCT07329933)
- Testing
- Dexamethasone, Dexmedetomidine, Dexamethasone and dexmedetomidine
- Where
- Egypt
- Volunteers
- 160 people
- Sponsor
- Benha University
Prostate Cancer, Urinary Bladder Cancer
Lung US for PEEP Optimization in Robotic Radical Prostatectomy or Cystectomy Patients
There is an increasing trend in the use of robotic-assisted radical prostatectomy or cystectomy (RARPC). Preventing lung atelectasis without inducing overdistention of the lung is challenging.
- Conditions
- Prostate Cancer, Urinary Bladder Cancer, Surgery, Positive End Expiratory Pressure
- Trial name
- NCT06307704
- Testing
- Lung Ultrasound - guided Stepwise PEEP, Standard Ventilation Protocol
- Where
- Egypt
- Volunteers
- 88 people
- Sponsor
- Nazmy Edward Seif
Adult Brain Tumor
Light Sedation or Intubated General Anesthesia in Patients With Brain Cancer Undergoing Craniotomy
This randomized clinical trial studies light sedation compared with intubated general anesthesia (a loss of feeling and a complete loss of awareness that feels like a very deep sleep) in reducing complications and length of…
- Trial name
- NCT02193568
- Testing
- Arm I (light sedation), Arm II (intubated general anesthesia)
- Where
- United States
- Volunteers
- 4 people
- Sponsor
- Ohio State University Comprehensive Cancer Center
LMA Vs I Gel
Randomized Comparative Study Between Classic Laryngeal Mask Airway and I Gel Airway in Obese Patients Having BMI 35-40 During Elective Non Abdominal Surgery.
Invistigators study both supraglottic airway devices; the classic LMA and the I GEL mask are satisfactory devices providing high airway leaking pressures.
- Trial name
- NCT03843827
- Testing
- Laryngeal Mask Airway, I gel Airway
- Where
- Egypt
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Cairo University
Coronary Artery Disease
Colchicine Protective Effect in Patients Undergoing Percutaneous Coronary Intervention (COLCHICINE-PROTECT)
The goal of this clinical trial is to evaluate the colchicine protective effect in patients undergoing Percutaneous Coronary Intervention (PCI).
- Trial name
- NCT05739929
- Testing
- Colchicine 0.5 MG Oral Tablet
- Where
- Egypt
- Volunteers
- 400 people
- Sponsor
- Helwan University
Fertility
Comparison of Sequential CFA vs CFA +rFSH for Elective Fertility Preservation.
This randomized was designed as non-inferiority trial aiming to compare the number of MII oocytes with 2-shot of Corifollitropin alpha (CFA) sequential administration: 150μg at stimulation day (SD) 1 and 100μg at SD 5 and 1-shot…
- Trial name
- 2-Shot (NCT06134479)
- Testing
- 150μg CFA (Elonva®) at stimulation day (SD) 1 and 100μg CFA(Elonva®) at SD 5, 150μg CFA (Elonva®) at SD 1 following by rFSH (Puregon®) 200IU daily from SD 8 until the day of the trigger
- Where
- Spain
- Volunteers
- 194 people
- Sponsor
- Fundación Santiago Dexeus Font
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