CompletedPhase 4

Postoperative Pain Relieve for Patients Undergoing Surgical Treatment of Femoral Fracture

Czechia82 participantsStarted 2023-09-04

Plain-language summary

The aim of the study is to investigate postoperative pain relief for patients undergoing surgical treatment of proximal femoral fracture using intrathecal administration of morphine.

Who can participate

Age range60 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: * signed informed consent * 60 to 90 years of age * surgical treatment of proximal femur fracture * The American Society of Anesthesiologists (ASA) classification I to III * spinal anesthesia used for the operation Exclusion Criteria: * general anesthesia used for the operation * allergy to opioids * high risk of respiratory depression

What they're measuring

Pain assessment

Timeframe: Every 2 hours after the surgery, total of 24 hours

Pain assessment during patient positioning

Timeframe: 24 hours

Time to administration of rescue medication

Timeframe: 24 hours

Total consumption of opioids on Intensive Care Unit

Timeframe: 24 hours

Trial details

NCT IDNCT05920642

SponsorUniversity Hospital Ostrava

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-07-29

View on ClinicalTrials.gov More Proximal Femur Fracture trials