Comparison Between Effect of Systemic Fentanyl Infusion and Fentanyl Added as An Adjuvant to Lidocaine in Bier Block For Controlling Pain in Patients Undergoing Hand Surgeries

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-40
SponsorAssiut University

About this trial

Injury and deformity of the upper extremity can result in dysfunction to nerves, tendons and bones which can lead to disability and pain.

Various techniques of regional anesthesia are frequently used for upper extremity surgery. Specifically, intravenous regional anesthesia, the Bier block, is an effective anesthetic technique. This technique, developed by Dr August Bier in 1908, provides complete anesthesia, a bloodless field, and eliminates the need for general anesthesia. However, it was not until the 1960s that this technique was reintroduced and used in upper extremity surgery due to several disadvantages and reports of major complications. Because of the dose of lidocaine and tourniquet time, there is potential for cardiac and neurological complications such as arrhythmias, seizures, and compartment syndrome the aim of this study To evaluate the effect of Systemic Fentanyl Infusion compared to addition of Fentanyl as An Adjuvant to Lidocaine in Bier Block for Controlling Pain in Patients Undergoing Hand Surgeries

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients age from 18 years to 40 years

Both sex

Patients of the American Society of Anesthesiologists (ASA) physical Status class I and II

BMI less than 40

Disqualifiers

• Patients who refuse to participate in study.

Uncooperative patients.

Patient with crush injury

Peripheral vascular, neurological or muscle diseases.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Fentanyl infusion

    Drug

    will received lidocaine with dose 250 mg and fentanyl infusion in dose of 200 µg in rate 10ml /hr using 50ml syringe pump.

  • Fentanyl Injection

    Drug

    will receive lidocaine 250 mg in addition to fentanyl injection in dose 100 µg by shots

Treatment groups

84 Participants
are divided into 2 treatment groups
Group A: group 1Experimental treatment 1 intervention
Group B: group 2Experimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

to compare intraoperative pain between systemic and local fentanyl using VAS score

pain will be assessed using an 11-point (0=no pain and 10=worst pain) VAS scale

Time frame
baseline

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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