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

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 hospitalizated in intensive care units

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT201303115866N7

Enrollment

Registered

2013-04-12

Start date

2013-03-14

Completion date

Unknown

Last updated

2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Symptoms, signs and abnormal clinical and laboratory findings. Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified

Interventions

Intervention 1: All three methods are used in all patients the first time suction with saline

if need suction, 3 cc of sterile saline and then using a suction catheter of the endotracheal tube, the patient is suctioned. Intervention 2: In the second round, if necessary, this time without the u

Prevention

Treatment - Drugs

All three methods are used in all patients the first time suction with saline

if need suction, 3 cc of sterile saline and then using a suction catheter of the endotracheal tube, the patient is suctioned.

In the second round, if necessary, this time without the use of normal saline and then suctioning using

If you need to suction the third time, the amount of liquid 2 ml - 2 ml pulled acetylcysteine ??in patients endotracheal tube is then suctioned.

Eligibility

Sex/Gender

All

Age

15 Years to 149 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAkram Sanagoo

Golestan University of Medical Sciences

a_sanagu@yahoo.com+98 17 1443 0360

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026