Duration of Blockade of Peripheral Nerves With Bupivacaine Depending of the Adjuvants

NCT04498923 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 68

Last updated 2022-04-13

No results posted yet for this study

Summary

The main aim of the investigator's study is to propose combination of local anesthetics and adjuvants that provides both adequate anesthesia during surgery and prolonged post-operative analgesia.

Conditions

  • Postoperative Pain
  • Peripheral Neuropathy
  • Fractures of the Upper Limb
  • Fracture of the Lower Limb (Except Hip), Initial Encounter
  • Intraoperative Hypotension
  • Intraoperative Hypertension
  • Pain Syndrome
  • Anesthesia
  • Anesthesia, Local
  • Local Anesthetic Systemic Toxicity

Interventions

DRUG

Bupivacaine, dexamethasone, epinephrine

Bupivacaine 75 mg, dexamethasone 4 mg, epinephrine 0,18 mg

Sponsors & Collaborators

  • Lviv National Medical University

    lead OTHER

Principal Investigators

  • Maksym Barsa · Сlinical resident

Eligibility

Min Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2022-04-05
Completion
2022-04-05

Countries

  • Ukraine

Study Locations

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Entities

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 NCT04498923 on ClinicalTrials.gov