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New treatment option for Postoperative Pain
Official title Effect of Posterior Femoral Cutaneous Nerve Block on Postoperative Posterior Lateral Knee Analgesia in Patients With TKA
ClinicalTrials.gov ID: NCT06522620
What this study is testing
- What it's testing
- The aim of this study was to observe the effects of posterior femoral cutaneous nerve block combined with sciatic and saphenous nerve block compared with sciatic and saphenous nerve block alone on postoperative posterior side of the knee (popliteal fossa) pain and sleep quality in patients with TKA, and to further alleviate postoperative posterior side of the knee pain in patients with TKA and improve the quality of postoperative sleep.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 45 to 80. Healthy volunteers may be eligible.
You may be able to join if
- Patients who are \>45 years of age; intended to undergo elective first TKA under general anesthesia
- ASA grade II-III.
- Agreed to participate in this study and signed the informed consent form.
- BMI less than 28Kg/m2.
You likely can't join if
- Patients who refuse to participate in the trial
- Preoperative inability to communicate due to speech and hearing impairment, etc.
- History of allergy to local anesthetics or opioids
- Contraindications to nerve block operation.
The study team makes the final eligibility decision.
Where it's taking place
- Yinchuan, Ningxia, China
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, 45 years to 80 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Yinchuan, Ningxia, China. 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.