The Efficacy of Combined Intrathecal Morphine and PENG Block on Postoperative Pain in Hip Arthrop… (NCT06298370) | Clinical Trial Compass
UnknownNot Applicable
The Efficacy of Combined Intrathecal Morphine and PENG Block on Postoperative Pain in Hip Arthroplasty
Turkey (Türkiye)3 participantsStarted 2024-03-18
Plain-language summary
This study aims to compare the postoperative 48-hour period in terms of morphine consumption, postoperative pain, and quality of recovery scores by combining the Pericapsular Nerve Group (PENG) block with low-dose intrathecal morphine in hip arthroplasty, as opposed to PENG alone and intrathecal morphine alone.
Who can participate
Age range
18 Years – 90 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:
* Aged between 18 and 90 years
* American Society of Anesthesiologists (score ranging from 1 to 4)
* Anterior hip arthroplasties
Exclusion Criteria:
* Patients with a history of opioid addiction
* Individuals under the age of 18
* Those aged 90 and above
* Allergies to morphine, fentanyl, bupivacaine, or tramadol
* Coagulopathy
* Infection at the injection site
* Severe cardiac, renal, or hepatic dysfunction
* Cases unable to provide informed consent
* Body Mass Index \>40 kg/m2
* Known neurological or anatomical deficits in the lower extremities
* Patients requiring a transition from spinal anesthesia to general 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.
What they're measuring
1
Morphine consumption
Timeframe: From end of anesthesia (15 minutes after anesthesia) to after 48 hours, up to 48 hours