Effects of Erector Spinae Plane Block and Intrathecal Morphine Administration on Intraoperative S… (NCT06693141) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effects of Erector Spinae Plane Block and Intrathecal Morphine Administration on Intraoperative Sevoflurane Consumption
Turkey (Türkiye)99 participantsStarted 2024-11-20
Plain-language summary
In our study, the investigators aimed to compare the intraoperative sevoflurane consumption and postoperative analgesic needs of patients who underwent lumbar disc herniation surgery and received either ESP block or ITM in the preoperative period with a control group.
Who can participate
Age range
18 Years – 65 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:
* Patients aged over 18 years
* Patients receiving general anesthesia
* Patients with an ASA score of I-II
* Patients undergoing elective surgery for single-level lumbar disc herniation
* Patients who provided informed consent after being informed
Exclusion Criteria:
Patients who did not provide informed consent after being informed
* Patients over 65 years of age
* Patients with an ASA score of III or higher
* Patients with recurrent lumbar disc herniation (LDH)
* Patients undergoing surgery for multi-level LDH
* Patients with a body mass index (BMI) of 30 or higher
* Patients with allergies to morphine or bupivacaine
* Patients with major cardiac, respiratory, hepatic, renal, neurological, or psychiatric diseases
* Patients with a history of alcohol or substance abuse
* Patients with a local infection at the injection site
* Patients with bleeding diathesis
* Patients with a history of anticoagulant medication use
* Patients with contraindications to spinal or regional anesthesia
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.