Evaluation the effects of Bupivacaine and dexmedetomidine on postoperative functional and pai

Phase 2

Completed

• Conditions: pain.; Generalized pain NOS; R52.9

• Registration Number: IRCT20160430027677N16
• Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 7 October 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

aged 20 to 70 years
American Society of Anesthesiologists physical status classification I and II
Absence of extensive damage to the rotator cuff

Exclusion Criteria

History of allergy to used drugs
The history of drug addiction
Known coagulation disorders
History of renal disease
History of liver disease
Body mass index more than 35 kg/m2

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.;Function. Timepoint: On the day before surgery and on postoperative day. Method of measurement: QoR-40 scoring system.

Secondary Outcome Measures

Name	Time	Method
Mean Arterial Blood Pressure. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: None Invasive Blood Pressure.;Mean pulse Rate. Timepoint: In recovery, 6, 12 and 24 hours after surgery. Method of measurement: Electrocardiogram.;Sleep disturbance. Timepoint: Until 24 hours after surgery. Method of measurement: Ten point scale.