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Taking people in PolandNo phase

Intravenous Dexamethasone (0 vs 4 vs 8 mg) as an Adjunct to PENG Block for Postoperative Analgesia in Total Hip Arthroplasty

Key facts

Where
Poznan, PolandSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 100 years old?

Source: NCT07581470, who can take part

Where in Poland

  • Poznan University of Medical SciencesPoznan, PolandContact: Malgorzata Reysner, M.D. Ph.D.Taking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Poznan University of Medical Sciences
Trial code
NCT07581470
Record updated
5 November 2026
Original description
his study will test whether giving dexamethasone through a vein can improve pain control after total hip replacement surgery. Dexamethasone is commonly used to reduce nausea and may also help with pain, but it is not clear which dose works best. Patients will be randomly assigned to receive either no dexamethasone, 4 mg, or 8 mg, in addition to standard anesthesia and a nerve block (PENG block). The main goal is to see how long patients go without needing additional pain medication after surgery. The study will also look at pain levels, use of opioid painkillers, nausea and vomiting, blood sugar levels, and possible side effects.Read full original descriptionShow less

Trial Evaluating Intravenous Dexamethasone (0 vs 4 vs 8 mg) as an Adjunct to PENG Block for Postoperative Analgesia in Total Hip Arthroplasty

his study will test whether giving dexamethasone through a vein can improve pain control after total hip replacement surgery. Dexamethasone is commonly used to reduce nausea and may also help with pain, but it is not clear which dose works best. Patients will be randomly assigned to receive either no dexamethasone, 4 mg, or 8 mg, in addition to standard anesthesia and a nerve block (PENG block). The main goal is to see how long patients go without needing additional pain medication after surgery. The study will also look at pain levels, use of opioid painkillers, nausea and vomiting, blood sugar levels, and possible side effects.

Inclusion: Age ≥ 18 years; Scheduled for elective total hip arthroplasty (THA); Planned use of regional anesthesia including PENG block; American Society of Anesthesiologists (ASA) physical status I-III; Ability to understand the study procedures and provide written informed consent; Ability to assess pain using the Numeric Rating Scale (NRS).

Exclusion: Chronic corticosteroid therapy or use of systemic steroids within 14 days prior to surgery; Significant immunosuppression (e.g., chemotherapy, biological therapy); Known hypersensitivity to dexamethasone or any component of the study medication; Active systemic infection or sepsis; Severe cognitive impairment or inability to reliably assess pain; Uncontrolled diabetes mellitus (e.g., HbA1c > 8.5% or baseline blood glucose > 200 mg/dL); Pregnancy or breastfeeding.

ClinicalTrials.gov NCT07581470