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PENG Block With or Without PPD Block for Postoperative Analgesia After Total Hip Arthroplasty

Sponsored by Kirsehir Ahi Evran Universitesi

About this trial

Last updated a month ago

Study ID

KAEAH-THA-PENG-PPD-01

Status

Not yet recruiting

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18+ Years
All Sexes

Trial Timing

Started 21 days ago

What is this trial about?

This single-center, prospective, randomized controlled clinical trial aims to compare the postoperative analgesic efficacy of PENG block with or without posterior pericapsular deep gluteal block in adult patients undergoing elective primary total hip arthroplasty under spinal anesthesia. Total hip arthroplasty is commonly associated with moderate to severe postoperative pain. Although PENG block provides analgesia for the anterior hip capsule, some patients may still experience pain originating from the posterior capsule. The addition of PPD block may improve analgesia by targeting posterior articular branches. Participants will be randomized into two groups: one group will receive PENG block, and the other group will receive PENG plus PPD block. Postoperative pain will be assessed using the Numeric Rating Scale (NRS). The study will compare postoperative pain scores and other analgesia-related outcomes between groups.

What are the participation requirements?

Inclusion Criteria

* Adults aged 18 years and older

* American Society of Anesthesiologists (ASA) physical status I-III

* Scheduled for elective primary total hip arthroplasty under spinal anesthesia

* Able to provide written informed consent

Exclusion Criteria

* ASA physical status IV or V

* Serious concomitant cardiac, respiratory, hepatic, or renal disease

* Known neuropsychiatric disorder

* Cognitive impairment preventing understanding or response to the Numeric Rating Scale (NRS)

* Coagulopathy

* Local anesthetic allergy

* Infection or scar at the block site

* Failed block

* Refusal to participate

* Signs of local anesthetic systemic toxicity after block

* Patients in the PENG plus PPD group who would be exposed to a total local anesthetic dose above 3 mg/kg in patients weighing less than 50 kg

* Revision total hip arthroplasty

* Total hip arthroplasty planned for fracture