CompletedNot Applicable

Hypobaric Spinal or Hyperbaric in Partial Hip Arthroplasty

Turkey (Türkiye)60 participantsStarted 2024-06-01

Plain-language summary

The aim of this study was to compare the effects of hypobaric and hyperbaric spinal applications on patient haemodynamics, duration of anaesthetic effect and postoperative analgesia. Thus, it was aimed to determine the method that protects haemodynamics more and suppresses postoperative pain complaints of patients better in this patient group with advanced age, comorbid systemic diseases and high risk of operation.

Who can participate

Age range18 Years – 65 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * ASA I-II * 18-65 aged Exclusion Criteria: * ASA III-IV * Deny to participiate * conditions that spinal anesthesia contraindicated * use of alpha or beta-blockers * allergy to local anesthetics * diabetes mellitus * peripheral vascular disease (The following exclusion criteria were added to ensure patient safety and to avoid confounding factors that could interfere with perfusion index measurements or hemodynamic responses: use of alpha or beta-blockers, diabetes mellitus, and peripheral vascular disease. These conditions may significantly alter autonomic regulation, vascular tone, or peripheral circulation, potentially affecting perfusion index values or increasing the risk of adverse reactions to spinal anesthesia)

What they're measuring

Visual analog pain score (VAS)

Timeframe: First postoperative 24 hours (The originally registered follow-up period of 3 months was entered in error. The intended and actual outcome assessment period for this study is the first 24 postoperative hours.)

Trial details

NCT IDNCT06417203

SponsorAdiyaman University Research Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-08-31