Clinical Trials Directory

Trials / Completed

CompletedNCT05892705

Intrathecal Dexmedetomidine to Decrease Postoperative Nausea and Vomiting and Shivering.

Can Subarachnoid Dexmedetomidine Decrease the Incidence of Postoperative Nausea and Vomiting and Shivering With Minimal Hemodynamic Instability in CS?

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Ain Shams University · Academic / Other
Sex
Female
Age
18 Years – 30 Years
Healthy volunteers
Accepted

Summary

Background: Highly selective α-2 agonist dexmedetomidine in increasingly used as an intrathecal adjuvant for caesarean section performed under subarachnoid block. Aim of the Study: The aim of the study is to determine whether low dose dexmedetomidine added to local anesthetic for spinal anesthesia will attenuate perioperative nausea and vomiting and shivering in lower segment caesarean section (LSCS) with minimal hemodynamic instability or not. Patients and Methods: Sixty parturients planned for elective CSs under spinal anesthesia were enrolled in this prospective controlled study and randomly divided into two equal groups. Spinal block was achieved with 10mg hyperbaric bupivacaine 0.5% plus 5µg dexmedetomidine (group D) (dexmedetomidine group) or 0.2 ml normal saline (group C) (control group). Hemodynamic parameters, incidence of nausea and vomiting and shivering were recorded. Keywords: Dexmedetomidine, Cesarean Section, Bupivacaine, Spinal Anesthesia, Shivering, PONV

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine Injection [Precedex]intrathecal injection of 5 mcg dexmedetomidine

Timeline

Start date
2021-06-01
Primary completion
2023-01-15
Completion
2023-01-15
First posted
2023-06-07
Last updated
2023-06-07

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05892705. Inclusion in this directory is not an endorsement.