CompletedPhase 4

PENG Block Versus LP Block for THA Postop Pain

United States154 participantsStarted 2022-06-13

Plain-language summary

The purpose of this randomized, double blinded, prospective study is to compare the postoperative analgesia provided by the PENG block to that provided by the LPB for patients undergoing primary anterior approach THA.

Who can participate

Age range18 Years – 90 Years

SexALL

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: * elective primary total hip arthroplasty surgery anterior approach * provided informed consent * no contraindications to medications used in providing the analgesic blocks Exclusion Criteria: * contraindications to regional anesthesia, such as an allergy to amide local anesthetics * pre-existing coagulopathy or thrombocytopenia \<100,000 * refusal of analgesic block for pain management * presence of an progressive lower extremity neurological deficit * localized or systemic infection * chronic use of high dose opioid analgesics (defined as daily use greater than 60 mg oxycodone equivalents) * pregnant * refusal of consent

What they're measuring

Numeric Rating Scale (NRS) Pain Score

Timeframe: hour 6

Trial details

NCT IDNCT05261009

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-07-20

Results submitted2024-01-10

View on ClinicalTrials.gov More Pain, Postoperative trials