Clinical trials: Day Surgery, active
Hip Fracture, Hip Fracture Surgeries
External Validation of Ten Prediction Models for 30-day Mortality Following Hip Fracture
This study aims to externally validate ten existing prediction models with a low risk of bias for 30-day mortality following hip fracture.
- Trial name
- PROTECT (NCT06961253)
- Where
- Netherlands
- Volunteers
- 3,500 people, healthy volunteers welcome
- Sponsor
- JointResearch
Bariatric Surgery Candidate
Evaluation of the Implementation of a Diet Workshop on the 15th Postoperative Day Following Bariatric Surgery
The objective of the study was to improve protein intake after the implementation of a dietary workshop performed on the 15th postoperative day following bariatric surgery.
- Trial name
- ADAPT (NCT05695040)
- Testing
- dietary workshop "proteins"
- Where
- France
- Volunteers
- 88 people
- Sponsor
- University Hospital, Clermont-Ferrand
Ankle Surgery
Quality of Recovery at Days 5-7 After Ankle Surgery: a Multicenter Study in Seine-Maritime
Ankle fractures are among the most common fractures in trauma care, with an estimated annual incidence of 100 to 150 per 100,000 inhabitants and a marked increase after age 40.
- Trial name
- QoR - CHEVILLE (NCT07814937)
- Testing
- Assessment of recovery quality on days 5-7 after ankle surgery
- Where
- 4 sites in France
- Volunteers
- 260 people
- Sponsor
- University Hospital, Rouen
Gynecological Day Surgery
The Effect of Remimazolam on Postoperative Sleep Quality
A large amount of clinical evidence shows that after surgery, especially major surgery, the sleep quality of patients often drops significantly immediately, with the most obvious decline on the first night after surgery, which…
- Trial name
- NCT07094945
- Testing
- Remimazolam, Propofol
- Volunteers
- 260 people
- Sponsor
- Tongji Hospital
Distal Radius Fracture Fixation
Same Day Discharge Vs. Hospitalization for Operative Fixation of Distal Radius Fractures
The goal of this clinical trial is to examine the results for same-day discharge after distal radius operative fixation in adult pupolation.
- Trial name
- NCT07276334
- Testing
- early release from hospital, Day after surgery release
- Where
- Israel
- Volunteers
- 70 people
- Sponsor
- Assaf-Harofeh Medical Center
Distal Radius Fractures
Impact of Early ADL Education on Outcomes Post DRF ORIF
This study is a randomized controlled trial (RCT). This RCT which will study the effect of performing daily activities early after a distal radius fracture being treated with surgical intervention of open reduction and internal…
- Trial name
- NCT06251206
- Testing
- ADL/Postoperative Instruction, Postoperative Instruction
- Where
- United States
- Volunteers
- 64 people, healthy volunteers welcome
- Sponsor
- George Washington University
Hip Fracture, Malnutrition
GNRI and Rectus Femoris Muscle Thickness in Older Patients Undergoing Hip Fracture Surgery
This prospective observational study will evaluate whether nutritional risk and reduced muscle mass are associated with postoperative outcomes in adults aged 65 years or older undergoing surgery for hip fracture.
- Conditions
- Hip Fracture, Malnutrition, Sarcopenia, Postoperative Complications
- Trial name
- NCT07751692
- Testing
- Geriatric Nutritional Risk Index Assessment
- Where
- Turkey (Türkiye)
- Volunteers
- 120 people
- Sponsor
- Fatih Sultan Mehmet Training and Research Hospital
Agitation, Postoperative Agitation
Effect of Daily Screen Time on Postoperative Emergence Delirium in Children Aged 2-11 Years
This prospective observational study aims to evaluate the association between daily screen exposure duration and postoperative emergence delirium in children aged 2 to 11 years undergoing elective lower abdominal surgery.
- Trial name
- NCT07552896
- Testing
- Daily Screen Exposure Duration
- Where
- Turkey (Türkiye)
- Volunteers
- 288 people
- Sponsor
- Kanuni Sultan Suleyman Training and Research Hospital
Surgical Wound
PICO 7 vs PICO 14 in Revision Hip and Revision Knee Surgery.
This is a single-site trial, and it has been designed to compare a revision hip cohort with a revision knee cohort. All consecutive eligible patients, under the care of participating Co-Investigator Orthopaedic Surgeons, are…
- Trial name
- NCT05389410
- Testing
- PICO 7, PICO 14
- Where
- United Kingdom
- Volunteers
- 164 people
- Sponsor
- Robert Jones and Agnes Hunt Orthopaedic and District NHS Trust
Colorectal Carcinoma, Day Surgery
Clinical Research on the Treatment Model of Ambulatory Surgery for Colorectal Cancer
To investigate the postoperative complication incidence and long-term efficacy between ambulatory surgery for colorectal cancer and traditional laparoscopic colorectal surgery in patients with colorectal tumor who are generally…
- Trial name
- NCT06637215
- Testing
- laparoscopic colorectal day surgery, traditional laparoscopic colorectal surgery
- Where
- China
- Volunteers
- 352 people
- Sponsor
- First Hospital of China Medical University
Knee Arthroplasty, Total
The Effect of Tele-Consultation Supported Education After Total Knee Arthroplasty Surgery
Following total knee arthroplasty, patients may encounter numerous problems that can hinder the performance of daily living activities, negatively impact quality of life, and increase morbidity and mortality rates.
- Trial name
- NCT06784596
- Testing
- Teleconsulting supported training
- Where
- Turkey (Türkiye)
- Volunteers
- 122 people
- Sponsor
- Turgut Sohret
Acute Postoperative Pain, Surgery
Continuous Versus Single Injection Adductor Canal Blocks for Outpatient Total Knee Arthroplasty
This is a single-center pilot study to determine if an adductor canal continuous nerve block is superior to single injection nerve block following total knee arthroplasty.
- Trial name
- NCT06784882
- Testing
- continuous peripheral nerve block with OnQ pump, single injection nerve block
- Where
- United States
- Volunteers
- 40 people
- Sponsor
- University of California, San Diego
Spinal Stenosis Lumbar
Evaluation of a Digital Person-Centered Rehabilitation Program Targeting Physical Activity in Spinal Stenosis Surgery (Get Back)
This study aims to investigate whether Get Back is more effective than standard rehabilitation in increasing the number of steps per day, improving physical activity levels, and functional ability for patients undergoing surgery…
- Trial name
- NCT06935201
- Testing
- Get Back
- Where
- 4 sites in Sweden
- Volunteers
- 252 people
- Sponsor
- Sophiahemmet University
Tonsillectomy, Infections
Head-Only Draping in Pediatric Tonsillectomy
This single-center, interventional study will compare 30-day postoperative infection rates in pediatric tonsillectomy performed with either head-only draping or traditional full-body draping.
- Trial name
- NCT07347301
- Testing
- Full-Body Surgical Draping, Head-Only Surgical Draping
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- NYU Langone Health
Obesity and Obesity-related Medical Conditions, Bariatric Surgery
Transition to Ambulatory Bariatric Surgery (TABS) Trial
This study will compare same day discharge and at least one night stay in the hospital after bariatric surgery. Patients undergoing bariatric surgery will be randomized (i.e. have an equal chance of either plan) to either group.
- Trial name
- TABS (NCT07011628)
- Testing
- Same Day Discharge
- Where
- United States
- Volunteers
- 200 people
- Sponsor
- Vanderbilt University Medical Center
Geriatric Patient Care Improvement
Effect of Postoperative Telehealth Counseling on Recovery and Self-Care in Geriatric Day Surgery Patients
This study was planned as a randomized controlled experimental study to evaluate the effect of postoperative telehealth counseling on patient outcomes in geriatric patients undergoing day surgery.
- Trial name
- NCT06892769
- Testing
- telehealth counseling
- Volunteers
- 72 people, healthy volunteers welcome
- Sponsor
- TC Erciyes University
Postoperative Urinary Retention (POUR)
Peri-operative Tamsulosin and Impact on Voiding Trial After Same-day Urogynecology Surgery
The purpose of this research study is to determine if taking tamsulosin preoperatively decreases your chances of being discharged after surgery with a Foley catheter (flexible tube that drains urine from the bladder into a…
- Trial name
- NCT06843538
- Testing
- Tamsulosin
- Where
- United States
- Volunteers
- 166 people
- Sponsor
- TriHealth Inc.
Health, Subjective, Cost Effectiveness
Effects of Patient-centered Telephone Education in Day Surgery
This study describe and evaluate the effectiveness of patient-centered telephone education in day surgery. The aim is to evaluate the effects of patient-centered telephone education on the experienced health of adult patients and…
- Trial name
- NCT03549403
- Testing
- Patient-centered telephone education
- Where
- Finland
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- University of Oulu
Lower Molar Requiring Extraction
Effect of Placing the Implant Crown on the Implant on the Same Day as the Implant vs. 4 Weeks Later.
In this study, participants with one lower first molar that require removal and replacement using dental implants will be enrolled.
- Trial name
- NCT04319042
- Testing
- Immediate Loading, Early Loading
- Where
- 2 sites in Switzerland
- Volunteers
- 100 people
- Sponsor
- University of Bern
Small Bowel Obstruction
Early Surgery Versus 3 Days Non-surgical Management in Acute Small Bowel Obstruction (SURGI-BOW)
For uncomplicated acute small bowel obstruction (aSBO), the "Bologna guidelines" recommend non-surgical management of 72 hours before considering surgery.
- Trial name
- SURGI-BOW (NCT06065150)
- Testing
- Standard support, Early surgery proposed according to the radiological score
- Where
- 14 sites in France
- Volunteers
- 630 people
- Sponsor
- University Hospital, Angers