CompletedNot Applicable

Comparison Effects of Two Regional Anesthetic Technique on Pain During High Risk Hip Fracture Surgery

Turkey (Türkiye)60 participantsStarted 2022-11-26

Plain-language summary

In this study, our is to compare effect of lumbosacral plexus and sacral plexus + suprainguinal fascia iliaca plane block on perioperative pain via analgesia nociceptive index monitor on high-risk patients undergoing hip fracture surgery.

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: * Patients over the age of 18 who will undergo hip surgery * ASA group 3-4 patients * Patients without allergies * Patients without psychiatric disorders * Patients without opioid dependence * Patients without severe liver and kidney failure * Patients without arrhythmia and beta-blocker use * Patients without contraindications for peripheral blocks Exclusion Criteria: * Patients who do not accept peripheral nerve block * Patients with failed peripheral nerve block * Patients scheduled for bilateral hip fracture surgery * Patients who have been operated on for hip fractures before * Patients with arrhythmia and beta-blocker use * Patients with contraindications for peripheral blocks * Chronic opioid consumption

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

effective analgesia control in patients with Analgesia Nociception Index (ANI)

Timeframe: postoperative 24 hour

Comparison of the Effects of Two Regional Anesthesia Techniques on Pain in High-Risk Hip Fracture Surgery with analgesia nociception index

Timeframe: postoperative 24 hour

Trial details

NCT IDNCT05862922

SponsorTC Erciyes University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-02-26

View on ClinicalTrials.gov More Pain trials

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.