Clinical trials: Surgical Complication
Postoperative Pain, Outpatient Surgery
A Before and After Study Studying the Impact of an Analgesia Protocol After Discharge From Outpatient Surgery
The goal of this before and after study is to measure the effectiveness of a home analgesia protocol after outpatient surgery in a tertiary hospital.
- Trial name
- NCT06268587
- Testing
- Measure the impact of the home analgesia protocol on the proportion of patients with a VAS > 3/10 on day one and who did not take analgesics.
- Where
- Belgium
- Volunteers
- 1,423 people
- Sponsor
- Centre Hospitalier Universitaire de Liege
Hydronephrosis
Clinical Significance of Supranormal Differential Renal Function in the Recovery of Hydronephrosis
The purpose of this study is to assess the clinical significance of supranormal differential renal function (DRF) in the recovery of unilateral hydronephrosis (HN) after surgery, pediatric patients who underwent pyeloplasty for…
- Trial name
- NCT01839006
- Testing
- dismembered pyeloplasty
- Where
- South Korea
- Volunteers
- 34 people
- Sponsor
- Seoul National University Hospital
Cervical Cancer
Surgery With or Without Chemotherapy in Treating Patients With Stage IB Cervical Cancer
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Giving chemotherapy drugs before surgery may shrink the tumor so that it can be removed during surgery.
- Trial name
- NCT00002536
- Testing
- cisplatin, vincristine sulfate, surgical procedure
- Where
- 41 sites in United States
- Sponsor
- Gynecologic Oncology Group
Pain, Postoperative, Surgery, Thoracic
Multimodal Analgesia in Children and Adolescents After the Ravitch Procedure and Thoracotomy
The study was performed in patients aged 6-18 years after the Ravitch procedure and thoracotomy. The primary aim of the study was to evaluate the efficacy and safety of pain control provided by the multimodal approach that…
- Trial name
- NCT03444636
- Testing
- Ropivacaine/Fentanyl, Bupivacaine/Fentanyl
- Where
- Poland
- Volunteers
- 94 people
- Sponsor
- National Institute for Tuberculosis and Lung Diseases, Poland
Pediatric Cancer, Neuroblastoma
Biomarkers of Resiliency In Childhood Cancer Surgery
This observational study is to better understand how children and their families recover after the stress of major surgery for cancer so that investigators can create ways to improve resilience during recovery.
- Conditions
- Pediatric Cancer, Neuroblastoma, Sarcoma, Wilms Tumor and Other Childhood Kidney Tumors
- Trial name
- BRICCS (NCT06674811)
- Testing
- Wearing Smartwatch, Patient Report Outcomes, Blood Draw
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Mayo Clinic
Pediatric Anesthesia, Postoperative Nausea and Vomiting (PONV)
Early Oral Fluid Intake in Children After Day Surgery
This study investigates the safety and tolerability of early oral clear fluid intake in children aged 1-8 years undergoing elective outpatient non-gastrointestinal surgeries.
- Conditions
- Pediatric Anesthesia, Postoperative Nausea and Vomiting (PONV), Ambulatory Surgical Procedures
- Trial name
- NCT06937684
- Testing
- Early Oral Fluid Intake, Traditional Oral Fluid Intake
- Where
- Turkey (Türkiye)
- Volunteers
- 172 people, healthy volunteers welcome
- Sponsor
- Ankara City Hospital Bilkent
Sickle Cell Disease
Is the Preoperative Preparation of Sickle Cell Patients Optimal: Assessment of Practices and Post-operative Complications
Children with sickle cell disease systematically receive a transfusion 2 to 5 days before scheduled surgery (with the exception of minor surgeries) in order to avoid post-operative complications of which the vaso-occlusive crisis…
- Trial name
- NCT04264871
- Where
- Belgium
- Volunteers
- 250 people
- Sponsor
- Queen Fabiola Children's University Hospital
Postoperative Complications
Intratracheal Dexmedetomidine Versus Lidocaine in Eye Surgery
Cough during emergence from general anesthesia is considered a critical event as it may lead to surgical bleeding laryngospasm hemodynamic instability and could be life-threatening in patients who are at risk of complications…
- Trial name
- NCT05291221
- Testing
- intratracheal saline, intratracheal Dexmedetomidine, intratracheal Lidocaine
- Where
- Egypt
- Volunteers
- 120 people
- Sponsor
- Minia University
Postoperative Nausea and Vomiting
Anti Emetic Efficacy of Combination of Ramosetron and Premixture of Naloxone With Patient-controlled Analgesia
Postoperative nausea and vomiting (PONV) is one of the most undesirable complications after general anesthesia, and may lead to increased hospital stay and health care costs.
- Trial name
- NCT02416115
- Testing
- Ramosetron, Naloxone, saline
- Volunteers
- 90 people
- Sponsor
- Kyungpook National University Hospital
Tonsillitis Chronic, Tonsillectomy
Tonsillectomy Using BiZact™ - a Randomized Side-controlled Clinical Trial
Tonsillectomies are frequently followed by severe postoperative pain, hence high analgetics consumption and prolonged hospitalization. Also, postoperative hemorrhages can be hazardous.
- Conditions
- Tonsillitis Chronic, Tonsillectomy, Hemorrhage, Postoperative Pain
- Trial name
- NCT03793816
- Testing
- BiZactTM Open Sealer/Divider
- Where
- Austria
- Volunteers
- 48 people
- Sponsor
- Medical University of Vienna
Persistent Spinal Pain Syndrome Type 2, Failed Back Surgery Syndrome
Open and Closed Loop DTM SCS in Patients With PSPS Type 2: ENDLESS Study
Evaluation of the effectiveness of differential target multiplexed spinal cord stimulation for treatment of Persistent Spinal Pain Syndrome Type II (PSPS-T2).
- Conditions
- Persistent Spinal Pain Syndrome Type 2, Failed Back Surgery Syndrome, Failed Neck Surgery Syndrome
- Trial name
- ENDLESS (NCT07211308)
- Testing
- Spinal Cord Stimulation
- Where
- 5 sites in Belgium, Netherlands
- Volunteers
- 200 people
- Sponsor
- Universitair Ziekenhuis Brussel
Preoperative Anxiety, Maladaptive Postoperative Behavior
Effects of Virtual Reality on Perioperative Pediatric Anxiety
This study evaluates the effect of virtual reality on anxiety levels in a pediatric surgical population. Half of participants will receive standard perioperative treatment, while the other half will receive additionally a virtual…
- Conditions
- Preoperative Anxiety, Maladaptive Postoperative Behavior, Emergence Delirium
- Trial name
- VIRTUALPED (NCT04043663)
- Testing
- Virtual Reality glasses, standard perioperative care without virtual reality program
- Where
- Spain
- Volunteers
- 240 people, healthy volunteers welcome
- Sponsor
- Germans Trias i Pujol Hospital
Delirium
Use of Dexmedetomidine in Children Undergoing Oral Maxillofacial Surgery to Decrease Emergence Delirium
The purpose of this study is to determine whether dexmedetomidine is effective in the treatment of emergence delirium of preschool children undergoing oral maxillofacial surgery.
- Trial name
- NCT01353378
- Testing
- dexmedetomidine
- Where
- China
- Volunteers
- healthy volunteers welcome
- Sponsor
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
Pelvic Organ Prolapse
Polypropylene Mesh in Prolapse Surgery
The purpose of this study was to report the long-term objective and subjective outcome after prolapse surgery with polypropylene mesh.
- Trial name
- NCT02383199
- Volunteers
- 161 people
- Sponsor
- Turku University Hospital
Patients With Adnexal Mass Prior to Surgery
Prospective Validation and Comparison of Different Ultrasound Methods for Discrimination Between Benign and Malignant Ovarian/Tubal Masses Prior to Surgery
The ability of different methods to discriminate between benign and malignant adnexal masses has been compared in a meta-analysis showing that the IOTA Simple Rules and the IOTA logistic regression model LR2 were superior to RMI…
- Trial name
- IOTA7 (NCT02847832)
- Testing
- Standardized transvaginal ultrasound examination
- Where
- Belgium
- Volunteers
- 1,700 people
- Sponsor
- KU Leuven
Emergence Agitation
Transition to Propofol After Sevoflurane Anaesthesia to Prevent Emergence Agitation
The aim of this randomized double-blinded study is to determine whether transition to propofol for 3 min at the end of sevoflurane anaesthesia reduces the incidence of EA in children undergoing genito-urinary paediatric surgeries.
- Trial name
- NCT03179293
- Testing
- Propofol, Normal saline
- Where
- Egypt
- Volunteers
- 70 people
- Sponsor
- Assiut University
Postoperative Nausea and Vomiting, Abdominal Pain
Bisacodyl Use in the Post-operative Care of Obstetrical/Gynecological (OB/GYN) Patients
The purpose of this study is to determine whether Bisacodyl, 5 mg usage decreases the incidence of nausea and abdominal pain after surgery, and also decreases the number of hospitalization days.
- Trial name
- NCT01011426
- Testing
- Bisacodyl
- Where
- United States
- Volunteers
- 285 people
- Sponsor
- Cooper Norcross Health
Incomplete Abortion
Sublingual Misoprostol Versus Standard Surgical Care for the Treatment of Incomplete Abortion
In this study, we will compare the safety and efficacy of 400 mcg sublingually administered misoprostol alone to standard surgical care for the treatment of incomplete abortion.
- Trial name
- NCT00466999
- Testing
- misoprostol, surgery
- Where
- 6 sites in Burkina Faso, Egypt and 3 more
- Volunteers
- 1,000 people, healthy volunteers welcome
- Sponsor
- Gynuity Health Projects
Pain, Postoperative
Gabapentin to Reduce Opioid Use Postoperatively (GROUP) in Children
The primary objective of this study is to determine if the peri and post operative use of gabapentin in children reduces the need for narcotics after thoracic surgery.
- Trial name
- NCT04724252
- Testing
- Gabapentin
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- University of California, Davis
Chronic Tonsillitis, Tonsillar Hypertrophy, Tonsillitis
Comparing Two Agents Used to Stop Bleeding During Tonsil Removal Surgery: Adrenaline Versus Hydrogen Peroxide
The goal of this quasi-experimental study is to compare the effectiveness of topical adrenaline and 3% hydrogen peroxide for controlling bleeding (hemostasis) during tonsil removal surgery in patients aged 5 to 18 years.
- Conditions
- Chronic Tonsillitis, Tonsillar Hypertrophy, Tonsillitis, Tonsillectomy
- Trial name
- NCT07675278
- Testing
- Adrenaline, Hydrogen Peroxide
- Where
- Pakistan
- Volunteers
- 64 people
- Sponsor
- Rawalpindi Medical College
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