Lidocaine vs. Lidocaine With Dexmedetomidine for Intravenous Regional Anesthesia (IVRA) in Upper Limb Surgery

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-60
SponsorFatima Memorial Hospital

About this trial

This study compares lidocaine alone vs. lidocaine with dexmedetomidine in Intravenous regional anesthesia (IVRA) for upper limb surgery in terms of pain scores and duration of analgesia

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

American Society of Anesthesiology Status I

American Society of Anesthesiology Status II

Elective surgery

Surgery duration <45 minutes

Disqualifiers

Sleep apnea

BMI >30

Heart block

uncontrolled hypertension

Trial design

Design model

Parallel

Treatments tested in this trial

  • Lidocaine (drug)

    Drug

    40 ml of 0.5% lidocaine

  • Dexmedetomidine

    Drug

    Dexmedetomidine (0.5 μg/kg)

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: LidocaineActive comparator 1 intervention
Group B: Lidocaine with DexmedetomidineExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Duration of Postoperative Analgesia

Time from surgery to first request for pain relief

Time frame
Up to 24 hours post surgery

Secondary outcomes

1

Pain Score according to Visual Analogue Scale (VAS)

Mean Pain Score according to Visual Analogue Scale (VAS) measured on a 0-10 scale, 0 being no pain at all and 10 meaning worst pain imaginable

Time frame
2 hours post-operation

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.