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New treatment option for Opioid Consumption, Postoperative
Official title Comparison of Pain Relief Methods for Hip Surgery: A Study on Two Different Nerve Block Techniques
ClinicalTrials.gov ID: NCT06821516
What this study is testing
- What it's testing
- This prospective randomized comparative study aims to compare the analgesic efficacy of pericapsular nerve group block (PENG) and lumbar erector spinae plane block (L-ESP) groups to relieve postoperative pain in participants over the age of 18 undergoing total hip arthroplasty under spinal anesthesia. The main question it aims to answer is: To demonstrate whether PENG block or L-ESP block is more effective in postoperative analgesia in patients undergoing total hip arthroplasty surgery based on pain scores, opioid consumption, and patient satisfaction.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Voluntary willingness to participate in the study.
- Patients who will undergo Total Hip Arthroplasty surgery.
- Patients aged over 18 years.
- ASA score I-II-III.
- Patients who are fully oriented and can cooperate.
You likely can't join if
- ASA score IV-V.
- Patients who refuse to participate in the study.
- Patients under 18 years of age.
- Presence of active infection in the area to be operated on.
- Chronic pain and continuous analgesic use.
- Patients with coagulation disorders.
See the full eligibility criteria
- Voluntary willingness to participate in the study.
- Patients who will undergo Total Hip Arthroplasty surgery.
- Patients aged over 18 years.
- ASA score I-II-III.
- Patients who are fully oriented and can cooperate.
- ASA score IV-V.
- Patients who refuse to participate in the study.
- Patients under 18 years of age.
- Presence of active infection in the area to be operated on.
- Chronic pain and continuous analgesic use.
- Patients with coagulation disorders.
- Patients who cannot cooperate with postoperative pain follow-up.
- Patients with allergies to local anesthetic agents.
- Presence of neuropathy or myopathy in the operated extremity.
The study team makes the final eligibility decision.
Where it's taking place
- Istanbul, Türki̇ye, Turkey (Türkiye)
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Istanbul, Türki̇ye, Turkey (Türkiye). Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.