Evaluation of Perioperative Anesthesia Requirements of Outpatient Cataract Patients
Investigation of Perioperative Anesthesia Requirements of Outpatient Cataract Patients Who Underwent Preoperative Anesthesia Evaluation.
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Contacts and Locations
Study Locations
-
-
-
İstanbul, Turkey, 34000
- Sağlık Bilimleri Üniversitesi Kanuni Sultan Süleyman Eğitim ve Araştırma Hastanesi
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
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
Sponsor
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- KAEK/2024.12.275
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.