The Prolonging Effect of Dexmedetomidine on Spinal Anesthesia Through Different Routes if Administrations

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18-80
SponsorKing Abdulaziz Medical City

About this trial

This prospective, double-blinded, randomized clinical trial aims to examine the effects of combining isobaric bupivacaine with dexmedetomidine administered intrathecally (IT), compared to the combination of isobaric bupivacaine administered intrathecally and dexmedetomidine administered intravenously (IV), on spinal anesthesia prolongation time in minutes, time of regression from Bromage score 3 to 0.

Eligibility criteria

Qualifiers

Male and female patients in adult age group more than 18 years old

ASA classification I, II, and III.

Orthopedic surgery, including total hip replacement (THR) and total knee replacement (TKR).

No history of Obstructive sleep apnea

Disqualifiers

Patient below 18 years old of both genders.

ASA classification of IV and more.

Patients with a height of less than 150 cm.

Patients on alpha-two antagonist ACE inhibitors and CCB.

Trial design

Treatments tested in this trial

  • Interventional group#1
  • Interventional group#2

Treatment groups

75 Participants
are divided into 3 treatment groups

Sponsors and collaborators