Comparison of tracheal intubation with propofol - remifentanil and propofol – succynylcholine in children 3 -12 years

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT201209089874N2

Enrollment

Registered

2013-08-11

Start date

2012-06-14

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

General Anesthesia. Other complications of surgical and medical care, not elsewhere classified

Interventions

Intervention 1: The intervention group, 3mg/kg propofol injection was used in 10 seconds, then 2microg/kg remifentanil injection is used in 30 seconds finally after 60 seconds, laryngoscopy and intuba

Diagnosis

The intervention group, 3mg/kg propofol injection was used in 10 seconds, then 2microg/kg remifentanil injection is used in 30 seconds finally after 60 seconds, laryngoscopy and intubation are perform

The control group, 3mg/kg propofol injection is used for 10 seconds, succynylcoline injection with 1.5mg/kg, after 50 seconds injected after 40 seconds, laryngoscopy and intubation are performed.

Eligibility

Sex/Gender

All

Age

3 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria:Children aged between 3-12 who undergoing elective surgery. Exclusion Criteria:Children with common cold; cardiorespiratory disease; nuromuscular disease; difficult intubation; other systemic disease

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Determination of tracheal intubation condition in children without muscle relaxant with propofol-remifentanil. Timepoint: 5 minutes before and after intubation. Method of measurement: Direct observation.	—

Secondary

Measure	Time frame
Comparing pulse rate and blood pressure in two groups. Timepoint: 5 minutes before and after intubation. Method of measurement: BP manometer, ECG.;Comparing laryngoscopy condition between two groups. Timepoint: During Laryngoscopy. Method of measurement: Direct observation.;Comparing cough between two groups. Timepoint: During and after intubation. Method of measurement: Direct observation.;Comparing movement of limbers between two groups. Timepoint: During and after intubation. Method of measurement: Direct observation.	—

Measure

Time frame

Comparing pulse rate and blood pressure in two groups. Timepoint: 5 minutes before and after intubation. Method of measurement: BP manometer, ECG.;Comparing laryngoscopy condition between two groups. Timepoint: During Laryngoscopy. Method of measurement: Direct observation.;Comparing cough between two groups. Timepoint: During and after intubation. Method of measurement: Direct observation.;Comparing movement of limbers between two groups. Timepoint: During and after intubation. Method of measurement: Direct observation.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Freshteh Naziri

Babol University Of Medical Sciences

freshteh.naziri@yahoo.com, ans_dep@yahoo.com+98 11 1223 8296

Outcome results

None listed

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