Comparison effects the Endotracheal suctioning with three methods,with installing normal saline serum,Installing N-acethylcycteine and without those on physiologic parameters and Amount of secretions at intubated patients

Not Applicable

• Conditions: Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified; Symptoms, signs and abnormal clinical and laboratory findings.; R00-R99

• Registration Number: IRCT201303115866N7
• Lead Sponsor: Research Deputy of Golestan University Of Medical Sciences, Gorgan, Iran

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

patients older than 15 years old; patient without intra cranial pressure; hemodynamics stability; patient without chronic obstruction pulmonary disease; patient without addiction; patient with Endotracheal tube; patient without severe heart failure. Exclusion criteria: existence tracheostomy tube; use of inotropic drugs; application of broncoscopy; septic shock; application of endotracheal suctioning in at least 2 hours.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Saturation of O2. Timepoint: Befor suction, 2 and 5 minutes after suction. Method of measurement: Pulse oximetry.;Blood pressure. Timepoint: Befor suction, 2 and 5 minutes after suction. Method of measurement: Sphygmomanometer.;Pulse rate. Timepoint: Befor suction, 2 and 5 minutes after suction. Method of measurement: Enumeration.;Respiratory rate. Timepoint: Befor suction, 2 and 5 minutes after suction. Method of measurement: Enumeration.