Clinical trials: Outpatient Surgery
Paediatric Outpatient Surgery
Reduction of Preoperative Anxiety in Children: Electronic Tab vs Midazolam
Rationale: The most frequently used means to prevent pre-anaesthetic anxiety in children is a drug premedication. Midazolam, a benzodiazepine, is mainly used.
- Trial name
- IPAD (NCT02192710)
- Testing
- electronic tab, Midazolam oral intake
- Where
- France
- Volunteers
- 118 people
- Sponsor
- Hospices Civils de Lyon
Hemorrhoid, Peri Anal Fistula
Discharge Conditions of Spinal Anesthesia With Heavy Prilocaine-Fentanyl and Heavy Bupivacaine-Fentanyl
In this prospective randomized study the investigators aimed to investigate difference of the duration of spinal anesthesia, discharge times and efficacy between low dose heavy Prilocaine-Fentanyl and heavy Bupivacaine-Fentanyl…
- Trial name
- NCT01880775
- Testing
- Prilocaine, Bupivacaine
- Where
- Turkey (Türkiye)
- Volunteers
- 50 people
- Sponsor
- Diskapi Teaching and Research Hospital
Ambulatory Surgery, Anesthesia
Effects of Propofol on Early Recovery of Hunger After Surgery
Recovery of hunger is a source of comfort for patients after general anesthesia. Moreover, this aspect of post-operative period is often required for discharging patients from hospital after ambulatory surgery.
- Conditions
- Ambulatory Surgery, Anesthesia, Energy Expenditure, Food Intake
- Trial name
- Propo-Faim (NCT02272166)
- Testing
- propofol, Sevoflurane
- Where
- France
- Volunteers
- 116 people
- Sponsor
- University Hospital, Rouen
Anxiety, Heart Rate Variability (HRV)
Anxiety and Physiological Responses in Ambulatory Surgery
This study aims to investigate the effects of music intervention on subjective anxiety and physiological indicators, including heart rate, blood pressure, and heart rate variability, in first-time ambulatory surgery patients, and…
- Conditions
- Anxiety, Heart Rate Variability (HRV), Heart Rate, Blood Pressure
- Trial name
- NCT07476820
- Testing
- Self-selected Music intervention, Fixed-music Music intervention
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- Da-Yeh University
Elective Surgery, Coughing
Efficacy of Propofol vs Placebo in the Prevention of Coughing During Emergence of General Anesthesia Under Desflurane
Emergence of general anesthesia is a critical period, in the same way as the induction of anesthesia, during which several adverse events may occur.
- Trial name
- PROPOREV (NCT02932397)
- Testing
- Intravenous dose of 0.5 mg/kg of propofol, Intravenous dose of 0.05 mL/kg of saline solution
- Where
- Canada
- Volunteers
- 154 people
- Sponsor
- Centre hospitalier de l'Université de Montréal (CHUM)
Regional Block for Pain Control, Supraclavicular Block
Duration of Analgesic Effect for Ultrasound Guided Supraclavicular Blocks With the Addition of Buprenorphine to Local Anesthetic Solution
The patients included will be those who have already agreed to have a brachial plexus nerve block for surgery. A flip of the coin will decide who gets and additive called buprenorphine in their block or not.
- Conditions
- Regional Block for Pain Control, Supraclavicular Block, Ultrasound Guided Block, Block Additive
- Trial name
- NCT01583179
- Testing
- Buprenorphine
- Where
- United States
- Volunteers
- 26 people
- Sponsor
- University of Wisconsin, Madison
Spinal Anesthesia
Spinal Anesthesia With Articaine and Lidocaine for Outpatient Surgery.
The purpose of this study is to compare two short-acting local anesthetics, articaine and lidocaine, for spinal anesthesia in day-case surgery.
- Trial name
- NCT00247741
- Testing
- spinal administration of articaine, spinal administration of lidocaine
- Where
- Netherlands
- Volunteers
- 80 people
- Sponsor
- St. Antonius Hospital
Postoperative Analgesia for Anterior Cruciate Ligament Surgery of the Knee
Analgesic Efficacy of Saphenous Nerve Blockade for Outpatient Knee Anterior Cruciate Ligament Surgery
The purpose of this study is to determine whether blockade of the saphenous nerve can provide the same degree of analgesia postoperatively for ACLS as a femoral nerve block without resulting motor blockade enhancing shortening of…
- Trial name
- NCT02071433
- Testing
- Saphenous nerve blockade, Femoral nerve blockade
- Where
- Netherlands
- Volunteers
- 58 people
- Sponsor
- Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Emergence Delirium, Pediatric Dental General Anesthesia
Pre-emptive Local Anesthesia and Emergence Behavior After Pediatric Dental General Anesthesia
This study will evaluate whether pre-emptive local anesthesia improves early recovery after ambulatory pediatric dental general anesthesia.
- Conditions
- Emergence Delirium, Pediatric Dental General Anesthesia, Postoperative Recovery
- Trial name
- PEDLA-QOR (NCT07604337)
- Testing
- Pre-emptive Local Anesthesia, Articaine Hydrochloride With Epinephrine
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people
- Sponsor
- seher orbay yasli
Bladder Cancer
Enhanced Recovery After Surgery (ERAS) for Ambulatory TURBT
This is a single-center, randomized-controlled trial to investigate the effectiveness of an ERAS protocol compared to usual care in patients with bladder cancer undergoing ambulatory TURBT.
- Trial name
- NCT05905276
- Testing
- ERAS Protocol, Standard of Care
- Where
- United States
- Volunteers
- 100 people
- Sponsor
- Johns Hopkins University
Breast Cancer
Comparison of Paravertebral Block With General Anesthesia in Patients Undergoing Breast Cancer Surgery
The purpose of this project is to determine if there is a difference between paravertebral block and general anesthesia in terms of time to discharge from the Post-Anesthesia Care Unit and pain level in patients undergoing…
- Trial name
- NCT00645138
- Testing
- Paravertebral Block, General Anesthesia
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- Weill Medical College of Cornell University
Healthy
Virtual Reality Educational Intervention for Nursing Students' Day Surgery Patient Counselling
This pilot feasibility study evaluates whether a virtual reality (VR) educational program can help nursing students develop better skills for counseling day surgery patients.
- Trial name
- CINDY (NCT07305714)
- Testing
- CINDY Virtual Reality Educational Intervention
- Where
- Finland
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Seinajoki University of Applied Sciences
Hemithyroidectomy, Outpatient
Randomized Investigation of Thyroid Operation as Day Surgery
hemithyroidectomy as a outpatient procedure is performed in some countries, it has never been done a RCT whether it is feasible
- Conditions
- Hemithyroidectomy, Outpatient, Hemmorhage
- Trial name
- NCT02891252
- Testing
- outpatient procedure
- Where
- Denmark
- Volunteers
- 86 people
- Sponsor
- Zealand University Hospital
Intraoperative Ventilation
A Comparison of Different Ventilation Strategies in Children Using the Proseal™ Laryngeal Mask Airway
The purpose of this research study is to compare difference between breathing by oneself or with the partial help from an anesthesia machine in children under general anesthesia.
- Trial name
- NCT00966433
- Testing
- Spontaneous ventilation, Pressure support Ventilation, Pressure control ventilation
- Where
- United States
- Volunteers
- 33 people
- Sponsor
- Wake Forest University Health Sciences
Obesity, Bariatric Surgery
Predictive Factors of Regain in Bariatric Patients Without Outpatients Care Regular.
The bariatric surgery is recommended for treatment of patients with severe obesity, resulting in greater weight loss and improvement of cardiovascular and metabolic comorbidities.
- Trial name
- Obesity (NCT04193384)
- Where
- Brazil
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Rio de Janeiro State University
Acute Pain, Surgery
Prescribing Vs. Recommending Over-The-Counter (PROTECT) Analgesics for Patients with Postoperative Pain:
This is a research project in which two standard of care practices will be evaluated to examine the difference in outcomes. The goal is to improve patient care and safety.
- Trial name
- PROTECT (NCT05370404)
- Testing
- Prescription by surgical team, Recommendation by surgical team
- Where
- United States
- Volunteers
- 250 people
- Sponsor
- University of Michigan
Surgery
Usability of SMART ANGEL Medical Device to Record and Transmit Health Data From Patient's Home Following Outpatient Surgery
This study represents the first step for testing this device in patients in real-life situations to evaluate the technological capacities and usability by the patient
- Trial name
- SMART ANGEL 1 (NCT03464721)
- Testing
- issued with SMART ANGEL device
- Where
- France
- Volunteers
- 30 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes
Ambulatory Patients in the Dep. of Medical Gastroenterology, Ambulatory Patients in the Dep. of Gynecology
Outpatients' Knowledge About and Attitude Toward Randomised Clinical Trials
The purpose of this study is to investigate the knowledge about randomised clinical trials and the attitude towards clinical research among Danish outpatients.
- Conditions
- Ambulatory Patients in the Dep. of Medical Gastroenterology, Ambulatory Patients in the Dep. of Gynecology, Ambulatory Patients in the Dep. of Orthopedic Surgery, Ambulatory Patients in the Dep. of Urology
- Trial name
- INFO-I (NCT03094598)
- Testing
- Leaflet, Brochure, Booklet
- Where
- 2 sites in Denmark
- Volunteers
- 428 people
- Sponsor
- Copenhagen Trial Unit, Center for Clinical Intervention Research
Hysterectomy
Day-case Versus Inpatient Laparoscopic Supracervical Hysterectomy
The purpose of this study is to determine if women subjected to laparoscopic supracervical hysterectomy in a day-case setting would be less satisfied with the length of hospital stay when compared with women who had an overnight…
- Trial name
- NCT01127243
- Testing
- day-case laparoscopic supracervical hysterectomy, inpatient LSH
- Where
- Norway
- Volunteers
- 49 people
- Sponsor
- Oslo University Hospital
Ambulatory Surgical Procedures
Effect of Dexmedetomidine on the Prevention of Emergence Agitation in Children Undergoing Day Surgery
Emergence agitation/delirium (EA/ED) is a common complication in pediatric surgery patients, which increases the risk of developing postoperative airway obstruction and respiratory depression.
- Trial name
- NCT03262090
- Testing
- 0.2ug/kg dexmedetomidine, 0.4ug/kg dexmedetomidine, 0.6ug/kg dexmedetomidine
- Where
- China
- Volunteers
- 389 people
- Sponsor
- Guangzhou Women and Children's Medical Center