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Effect of Psychosocial and Psychophysical Factors and Preemptive Analgesia on Postoperative Pain in Upper Limb Surgery

NCT05248152 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 90

Last updated 2022-02-21

No results posted yet for this study

Summary

The purpose of this study is to define the role of preemptive systemic analgesia in combination with regional anesthetic techniques on postoperative pain following upper limb surgery in different subgroups of patients with different psychosocial and psychophysical characteristics.

Conditions

  • Postoperative Pain

Interventions

COMBINATION_PRODUCT

Paracetamol and Ibuprofen

Patients will receive paracetamol 1g and ibuprofen 400 mg before surgical incision.

DRUG

Pregabalin 150mg

Patients will receive pregabalin 150 mg in the hour before surgery

DRUG

Placebo

Patients will receive a placebo capsule in the hour before surgery and two intravenous doses of saline before surgical incision.

Sponsors & Collaborators

  • University Medical Centre Ljubljana

    lead OTHER

Principal Investigators

  • Benjamin Jonke, M.D. · University Medical Centre Ljubljana

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-01-13
Primary Completion
2024-01-13
Completion
2024-04-13

Countries

  • Slovenia

Study Locations

More Related Trials

Entities

Drugs

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 NCT05248152 on ClinicalTrials.gov