Actively Recruiting

Phase 4
Age: 60Years +
All Genders
NCT07378215

The Effect of Corticosteroids on Quality of Life Following Total Hip Arthroplasty: HIPSTER Study

Led by Ziekenhuis Oost-Limburg · Updated on 2026-04-08

224

Participants Needed

2

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Total hip arthroplasty (THA) is a highly effective and commonly performed procedure for end-stage osteoarthritis. Perioperative inflammation contributes to postoperative pain, fatigue, and delayed recovery. Dexamethasone, a potent glucocorticoid with strong anti-inflammatory properties, is widely used in orthopedic surgery and incorporated into Enhanced Recovery After Surgery (ERAS) protocols for THA to reduce pain, PONV, and fatigue. While intermediate doses of dexamethasone (25 mg) are considered safe and beneficial in the short term, their long-term effects on health-related quality of life and persistent pain remain unclear. Therefore, the main objective of the HIPSTER trial is to evaluate the effect of different doses of a single intraoperative intravenous dose of dexamethasone (5 mg versus 25 mg) on health-related quality of life up to three months after surgery.

CONDITIONS

Official Title

The Effect of Corticosteroids on Quality of Life Following Total Hip Arthroplasty: HIPSTER Study

Who Can Participate

Age: 60Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • aged 60 years or older;
  • scheduled for elective total hip arthroplasty;
  • procedure under spinal anaesthesia.
Not Eligible

You will not qualify if you...

  • hip revision surgery (reoperation);
  • bilateral total hip arthroplasty during the same procedure;
  • known hypersensitivity to dexamethasone or other corticosteroids;
  • chronic systemic use of corticosteroids, defined as daily corticosteroid therapy for > 4 weeks within the last 3 months, with anticipated need for a perioperative stress dose of corticosteroids;
  • active gastric of intestinal ulcers;
  • lack of informed consent or inability to give informed consent;
  • urgent, non-elective surgery.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Ziekenhuis Oost-Limburg

Genk, Limburg, Belgium, 3600

Not Yet Recruiting

2

Ziekenhuis Oost-Limburg

Genk, Belgium

Actively Recruiting

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Research Team

S

Steven Thiessen

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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