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Volume Effect in Peng Block for Total Hip Replacement

NCT06427551 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2024-05-24

No results posted yet for this study

Summary

This study is to investigate whether a different volume of ropivacaine, with the same prescribed dosage based on body weight, can affect block efficacy, duration and side effects in the first 24 hours postoperatively.

Conditions

  • Anesthesia
  • Post Operative Pain

Interventions

DRUG

Ropivacaine

The local anesthetic was dosed on the patient's weight (50-59kg: 120mg, 60-61kg: 140mg, 70-79kg: 160mg, ≥80kg: 180mg)

Sponsors & Collaborators

  • Azienda Ospedaliero, Universitaria Pisana

    lead OTHER

Principal Investigators

  • manuela nicastro, MD · aoupisa

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-01-01
Primary Completion
2024-01-30
Completion
2024-01-30

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06427551 on ClinicalTrials.gov