Elective Surgery

9

Review clinical trials related to Elective Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Median Nerve Electromyography to Monitor Intraoperative Neuromuscular Function

The effect of muscle relaxants need to be followed during surgery and before waking up the patient, the anesthesiologist has to make sure that the effect of muscle relaxants is gone. For this purpose, anesthesiologists use so called objective neurlmuscular monitors. These monitors stimulate the ulnar nerve in the wrist and examine the evoked muscle response. The aim of this study is to examine the usability of another nerve in the wrist, the median nerve.

Participants needed: 45
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Pongrácz AdriennUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

ASA I-III physical status [+3]

neruomuscular disorder in patient history (eg. stroke, myasthenia) [+7]

Status: Recruiting

Surgical COrncerns and Psychological Evaluation of Patients Undergoing Elective Surgery

This study wants to obtain more information regarding the patient's concerns since concerns of the patient about the procedure is found as a predictor for the development of chronic post-surgical pain. This step is crucial in translating early identification of a high-risk population into preventive policies. Using a semi-structured interview, the investigators aim to gather this additional information, which is essential in the development of an (individualized) biopsychosocial care pathway in the future.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, AntwerpUpdated: Apr 29, 2026Locations: 1
Eligibility criteria

≥ 18 years old [+5]

Diagnostic procedures requiring anaesthesia

Status: Recruiting

Validity of Frailty Screening Tools as a Measure for Postoperative Outcomes

Frailty is a common geriatric syndrome defined as a clinical state of decreased physiologic reserve resulting in increased vulnerability to stressors. It is associated with several unfavorable postoperative complications independent of age such as readmission, length of hospital stay and mortality. To address these concerns, medical societies have acknowledged a need for routine screening to identify elderly patients who are at high risk for major complications before undergoing surgery. In the absence of a golden standard for frailty assessment, there are multiple assessment tools available. However, the challenge with many frailty tools is that they can be time-consuming, and require expertise and clinical training.This poses a challenge for screening a large elderly population before surgery. Some frailty assessment tools, such as PRISMA7 (The Program of Research to Integrate Services for the Maintenance of Autonomy), timed up and go (TUG) and the clock drawing test (CDT), have been demonstrated to be quick, simple and easy to use with minimal training. The PRISMA-7 is a frailty screening questionnaire that consists of seven dichotomous items considering age, gender, health problems that affect activities of daily living (ADLs), assistance from others with ADLs, having to count on someone if needed, and the use of mobility aids. The TUG test is used for assessing fall risk and frailty in older patients. It is measured by the time it takes an individual to stand up from a seated position, walk three meters and return back to a seated position. There is no standard cut-off for TUG, however, a cut-off of \> 10 seconds has been used to identify frailty. Cognitive impairment in older surgical patients may predispose patients to executive dysfunction that many elderly patients experience postoperatively and has shown to be a risk factor for surgical complications. Some studies suggest a strong relationship between cognitive impairment and physical frailty resulting in cognitive frailty when evaluating older adults.The CDT has shown to be a valuable screening tool for cognitive concerns. When administering the CDT, a patient receives instructions to draw a clock. Performing the test requires auditory comprehension, planning, sustained attention, visual-spatial skills and executive skills. The prevalence of surgical frailty in Iceland has not been researched thoroughly enough to provide an accurate estimate. This is important to reveal the number of senior surgical patients at high risk of adverse postoperative outcomes who could benefit from a preoperative intervention. However, there is a lack of consensus on an optimal frailty assessment to screen patients for identifying frail patients prior to surgery, and more research is needed to evaluate which group of patients would benefit the most from prehabilitation. The scientific value of this study is to elucidate the extent of frailty risk and its associated postoperative outcomes in older surgical patients undergoing elective surgery. We opt to find a convenient screening routine prior to surgery to identify patients at risk of frailty. Therefore, the study aims to validate three frailty screening methods and to assess a positive screening result as an independent risk factor for adverse postoperative outcomes in a cohort of elderly surgical patients undergoing elective surgery. We hypothesize that elderly patients at risk of frailty have a higher rate of surgical complications than patients not at risk of frailty. Patients aged ≥ 70 years who undergo elective surgery will be prospectively examined at the Department of Anesthesiology and Critical Care of Landspítali. The screening assessments to be evaluated are the Program of Research to Integrate Services for the Maintenance of Autonomy (PRISMA-7), a combination of Timed Up \& Go (TUG), Clock Drawing Test (CDT) and the FRAIL questionnaire, and a combination of PRISMA-7, TUG and CDT. Additional clinical data and outcomes will be obtained from the electronic medical records of Landspítali. The postoperative outcomes measured will be 180-day mortality, surgical complications, 90-day readmission, delirium, non-home discharge and length of hospital stay. Patients who screen positive on the CDT (≤ 2/3 points) and TUG (≥ 11 seconds) will be considered frail. Those who do not screen positive on both of these tests will be part of the control group (non-frail).

Participants needed: 350
Trial details
Age: 70+Biological sex: AllType: ObservationalSponsor: University of IcelandUpdated: Jan 26, 2026Locations: 1Duration: 1 Year
Eligibility criteria

Patients ≥ 70 years who present for preoperative work-up at the anesthesia depar... [+1]

Not undergoing planned surgery

Status: Recruiting

Virtual Group Prehabilitation Education (Surgery School) Feasibility Trial

One in four patients requiring planned major surgery have complications. Prehabilitation; which involves increasing physical activity, improving nutrition and supporting emotional well-being prior to surgery can reduce these complications and improve recovery. Group preoperative prehabilitation classes (surgery schools) are advocated by the Centre for Perioperative Care and are standard care in many hospitals, despite a lack of evidence for their effectiveness in improving patient outcomes. In phase 1 an 2 of this research investigators used patient experiences and co-participatory methods to optimise an existing intervention to make it as acceptable and as engaging as possible. The resulting education package is called 'GoPREPARE' Investigators now intend to test the practicalities of trialing GoPREPARE on preoperative patients with cancer. 24 patients awaiting surgery will be recruited from University Hospital Plymouth and randomly allocated equally to: Group - GoPREPARE and Group 2- standard care. Participants will complete lifestyle questionnaires before during and after their hospital stay. To evaluate the experience, \~8 participants will be interviewed. 5 clinical staff involved in the trial will also take part in a focus group. The information collected will be analysed to assess if it is feasible to conduct a larger trial.

Participants needed: 24
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital Southampton NHS Foundation TrustUpdated: Dec 12, 2025Locations: 1
Eligibility criteria

Adults undergoing elective surgery for any body cavity cancer with curative inte... [+2]

Children [+5]

Status: Recruiting

Perioperative Immunonutrition Under Enhanced Recovery After Surgery

The goal of this clinical trial is to compare the effect of perioperative immunonutrition supplement in gynecologic cancer patients. The main questions it aims to answer are: * is there any difference in the nutritional outcomes and functional outcomes between intervention and conventional groups? * is there any difference in the post-surgical outcomes between intervention and conventional groups? Participants (intervention) will be provided the immunonutrition supplement before and after operation. Researchers will compare intervention group with conventional group to see if there is any difference in postoperative outcomes.

Participants needed: 106
Trial details
Age: 18-80Biological sex: FemaleType: InterventionalSponsor: Universiti Putra MalaysiaUpdated: Aug 19, 2025Locations: 1
Eligibility criteria

Those who diagnosed with GC [+1]

Those are involved gastrointestinal tract (complication) [+3]

Status: Recruiting

Carotid Artery Corrected Flow Time and Inferior Vena Cava Collapsibility Index for Prediction of Hypotension After Induction of General Anesthesia in Geriatric Patients Undergoing Elective Surgery

In this observational study, we will assess cFT by Carotid ultrasound and IVC collapsibility index for prediction of hypotension after induction of general anesthesia in geriatric patients undergoing elective surgery.

Participants needed: 189
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Jul 1, 2025Locations: 1
Eligibility criteria

American Society of Anaesthesiologists Physical Status I to Ⅱ [+2]

• patients who refused to participate in the study [+7]

Status: Not yet recruiting

Impact of Total Coronary Revascularization Via Left Anterior Thoracotomy (TCRAT) vs. Robotic-Assisted Harvesting of LIMA (ITcrats)

The two types of total coronary revascularization via left anterior thoracotomy (TCRAT) might have their potential benefits and disadvantages. The proposed randomized clinical trial here will compare 'RA-TCRAT' with 'Nonrobotic TCRAT' procedures concerning effects on hospital stays, overall healthcare costs, safety, and feasibility. If the two TCRAT procedures are comparably effective and safe, the 'Nonrobotic TCRAT' procedure is probably preferred as it seems easier to use. However, if the 'Nonrobotic TCRAT' procedure is less effective and less safe than the "robotic TCRAT,' that procedure should be preferred.

Participants needed: 182
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mohamed R El TahanUpdated: Jun 4, 2025Locations: 1
Eligibility criteria

Scheduled for any type of elective minimally invasive coronary revascularization... [+2]

Planned for coronary revascularization surgery without CPB; [+9]

Status: Recruiting

Ultrasonographic Airway Assessment in Predicting Difficult Laryngoscopy in Pediatric Patients Undergoing Elective Surgery

This study aims to evaluate the diagnostic accuracy of ultrasonographic airway examination in predicting difficult laryngoscopy in pediatric patients undergoing elective surgery.

Participants needed: 308
Trial details
Age: 2-5Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Nov 1, 2024Locations: 1
Eligibility criteria

Children aged (2-5) years old. [+3]

Maxillofacial trauma [+3]

Status: Recruiting

Gastric Ultrasound in Elective Surgical Diabetic Patients

The aim of this study is to evaluate the role of gastric ultrasound in elective surgical diabetic patients.

Participants needed: 130
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Tanta UniversityUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

Age ≥ 18 years. [+2]

American Society of Anesthesiology (ASA) physical status >III. [+7]