- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06824935
Evaluation of Perioperative Anesthesia Requirements of Outpatient Cataract Patients
February 7, 2025 updated by: Naime Yalçın
Investigation of Perioperative Anesthesia Requirements of Outpatient Cataract Patients Who Underwent Preoperative Anesthesia Evaluation.
According to the literature, preoperative evaluation has been shown in studies to be the first step in ensuring that patients' anesthesia care is carried out safely.
In cataract surgery, which is a day anesthesia procedure frequently observed in the geriatric population, topical-local anesthesia is mostly applied.
It is believed that preoperative anesthesia evaluation will be beneficial due to the complications that may develop during the procedure, patient safety and therefore the duration of postoperative hospital stay.
The aim of the study is to evaluate patients who may need anesthesia intervention among patients whose preoperative anesthesia evaluations have been completed due to the possibility of consultation from the anesthesia department if necessary for patients who will undergo cataract surgery with local-topical anesthesia.
Study Overview
Status
Enrolling by invitation
Intervention / Treatment
Detailed Description
Preoperative assessment is the first step in ensuring that patients receive safe anesthesia care.
Over time, this process has changed significantly from an era when patients were admitted to the hospital the night before surgery to a time when the majority of patients, including those scheduled for major surgical procedures, arrive on the day of surgery.
Outpatient preoperative assessment clinics are private and academic practices that require training in institutional staff; although common, the optimal model is unknown and may depend on the characteristics of the hospital, such as the specific types of care provided, geographic and socioeconomic differences in the population served by the hospital, patient expectations, and facility availability.
The American Society of Anesthesiologists physical status (ASA-PS) classification provides a starting point for triage.
Outpatient surgery may be safe even in patients with a high ASA-PS classification.
A multicenter European study of 57,709 procedures including ASA PS III patients found that major complications such as stroke, myocardial infarction (MI), and pulmonary embolism were extremely rare and were not clearly associated with any deaths.
Cataract surgery is the most frequently performed day surgery, with an estimated 3.3 million procedures performed annually by 2020 and 4.4 million by 2030.
Almost all are performed in an outpatient setting with minimal intravenous sedation and different local anesthesia methods.
The frequency of unplanned hospitalization on the day of surgery is estimated to be 0.05%.
The majority of anesthesia interventions are related to the treatment of hypertension or bradycardia.
Hypertension is often associated with anxiety and is often treated with sedation.
Rarely, bradycardia requiring treatment typically occurs as a vagal response or following intravenous sedation.
Considering the geriatric population and associated medical problems, monitored anesthesia care with anesthesia personnel may be considered more reliable in cataract surgery.
Studies have reported that the rate of anesthesia call represents 3.4% of interventions, similar to those reported in the last 15 years, but some authors have reported higher anesthesia call rates of over 20%.
In literature stated that the lack of premedication probably contributed to this increase, and that other factors such as the lack of anesthesia consultation, the level of information given to the patient, the definition of the criteria for calling the anesthesiologist, and the technique applied for topical anesthesia may have also affected the rates.
The studies supported the need for anesthesia personnel to be present in the operating room to be evaluated by anesthesia personnel during cataract surgery by citing the study in 406 cases, in which the rate of anesthesia requirement during peribulbar anesthesia was shown as 28.5% and interventions were typically directed towards arrhythmia, agitation, or hypertension.
The primary aim of this study was to evaluate patients who may need interventions in terms of anesthesia and reanimation among those who have completed preoperative anesthesia evaluations due to the possibility of consultation with the anesthesia department if needed in patients who will undergo cataract surgery under local-topical anesthesia.
Investigator's secondary aim is to analyze the frequency of anesthesia interventions needed and the risk factors that play a role in these interventions by examining patient data, accompanied by patients' demographic data, medical history and preoperative anesthesia examinations.
Study Type
Observational
Enrollment (Estimated)
470
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
İstanbul, Turkey, 34000
- Sağlık Bilimleri Üniversitesi Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who will undergo local cataract surgery in the ophthalmology clinic by applying to our hospital's anesthesia polyclinic
Description
Inclusion Criteria:
- Being over 18 years old, ASA I-IV status, and undergoing cataract surgery under local-topical anesthesia
Exclusion Criteria:
- If the procedure is performed under general anesthesia or sedation, emergency surgery or ASA-E
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number and nature of anesthesia requirements in local cataract surgery
Time Frame: Up to 8 weeks after registration
|
Patients will be examined with parameters such as age, gender, weight and height will be combined to report BMI in kg/m^2, history of chronic disease, history of medication, smoking, alcohol, allergy, previous eye surgery, ASA, type of surgical anesthesia, reasons for anesthesia requirement, increasing oxygen flow rate, clarifying ECG, opening i.v.
access, sedation, general anesthesia, additional medication, and length of hospital stay.
|
Up to 8 weeks after registration
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 2, 2025
Primary Completion (Estimated)
May 2, 2025
Study Completion (Estimated)
July 2, 2025
Study Registration Dates
First Submitted
January 29, 2025
First Submitted That Met QC Criteria
February 7, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
February 7, 2025
Last Verified
February 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KAEK/2024.12.275
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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