? Comparing dexmedmotidine and remifentanil to reduce pain in disc

Phase 2

Recruiting

• Conditions: Disc herniation.; Traumatic rupture of lumbar intervertebral disc, sequela; S33.0XXS

• Registration Number: IRCT20141209020258N108
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 May 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 96

Inclusion Criteria

Both gender
ASA class 1 and 2
Candidate surgery of hernia disc
No allergy to drug use
No addiction

Exclusion Criteria

Dissatisfaction
Allergy to drug use

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: Recovery, 2 and 4 and 6 and 12 hours after surgery. Method of measurement: Visual analog scale.;Relaxation. Timepoint: 24 hours after surgery. Method of measurement: Ramsy score.