Controlled Sedoanalgesia in External DCR Surgery (NCT05397301) | Clinical Trial Compass
CompletedNot Applicable
Controlled Sedoanalgesia in External DCR Surgery
Turkey (Türkiye)44 participantsStarted 2020-02-07
Plain-language summary
In our study, we aim to compare general anesthesia and controlled sedoanalgesia methods in dacryocystorhinostomy (DCR) surgery in terms of hemodynamic data, bleeding amount, postoperative complications (bleeding, pain, etc.) and anesthesia satisfaction in a prospective and randomized controlled manner.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Primary DCR surgery to be performed
* 18 years and older patients
* Having an American Society of Anesthesiology score of 1, 2, 3
* Having approved and signed the informed consent form
Exclusion Criteria:
* Patients younger than 18 years old
* Patients with an American Society of Anesthesiology score of 4 and above
* Patients who do not accept informed consent
* History of drug allergy and opioid tolerance
* Uncontrolled diabetes mellitus
* Coagulation disorder
* Cases with severe liver and kidney disease
* Those who refused to participate in the study
* They will have DCR surgery again
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
hemodynamic data
Timeframe: through surgery completion
2
hemodynamic data
Timeframe: through surgery completion
3
hemodynamic data
Timeframe: through surgery completion
4
amount of bleeding
Timeframe: amount of bleeding calculated during surgery
Trial details
NCT IDNCT05397301
SponsorTurkish Society of Anesthesiology and Reanimation