Comparison of the effect of different doses of intrathecal Ropivacaine in surgery

Phase 2

Completed

• Conditions: Spinal anesthesia using ropivacaine.; Other complications of anesthesia; T88.5

• Registration Number: IRCT20211017052786N4
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

Iranian race
Patients with American Stroke Association (ASA) grade 1, 2
Umbilical cord surgeries
Age over 18 and under 65 years

Exclusion Criteria

Allergy to amide drugs
Pregnancy
History of substance abuse
Heart rate less than 60 beats per minute at rest

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
evels of sensory and motor block. Timepoint: In minutes 15,10,8,8,6,4,2. Method of measurement: Motor nerves using voice commands for the patient and Pinprick of skin to observe the sensory nerve response.