About this trial
This study aims to investigate the efficacy of adding a Posterior Pericapsular Deep gluteal block to two other standard nerve blocks-the Pericapsular Nerve Group block and the Lateral Femoral Cutaneous Nerve block-for patients undergoing orthopedic hip surgery. While standard blocks target the front of the hip, many patients still feel pain in the back (posterior) of the joint. Researchers will compare two groups of patients to see if this triple-block combination provides better pain relief and reduces the need for rescue opioid medications in the 24 hours following surgery.
Eligibility criteria
Qualifiers
Age greater than or equal to 18 years.
Both genders included.
American Society of Anesthesiologists (ASA) physical status classification I-III.
Undergoing elective orthopedic hip surgery.
Disqualifiers
Patient refusal of procedure or participation.
American Society of Anesthesiologists (ASA) physical status classification IV.
Allergy to any of the drugs used in the study.
Local skin infection at the injection site.
Trial design
Treatments tested in this trial
- Posterior Pericapsular Deep Gluteal, Pericapsular Nerve Group, and Lateral Femoral Cutaneous Nerve Blocks.
- Pericapsular Nerve Group and Lateral Femoral Cutaneous Nerve Blocks.