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The frequency of laryngospasm in two different methods of ostoperative tonsillar anesthesiay

Frequency of laryngospasm in two different methods of No touch and HDDE (Head Down Deep Extubation) after tonsillectomy and adenotonsillectomy in children

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191006044995N1
Enrollment
42
Registered
2020-04-06
Start date
2018-04-21
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Condition 1: Hypertrophy of tonsils. Condition 2: Laryngeal spasm. Hypertrophy of tonsils Laryngeal spasm

Interventions

Intervention 1: Intervention group: All patients will receive standard general anesthesia with propofol (3-5 mg / kg) and atracurium (0.5 mg / kg) to easier intubation. After induction, ondansetron (0

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 15 Years

Inclusion criteria

Inclusion criteria: Ages 5 to 15 years of age both male and female with ASA Class I, II People who require tonsillectomy or adenotonsillectomy based on a doctor's diagnosis. No diet and no supplement consumption No specific sport activity Volunteers willing to cooperate

Exclusion criteria

Exclusion criteria: People with a history of asthma People who have had a history of problems with intubation or extubation.

Design outcomes

Primary

MeasureTime frame
SPO2 is expressed as a percentage. Timepoint: SPO2 levels were recorded in both groups at 0, 5 min, 10 min, 15 min and 2 h after extubation. Method of measurement: Pulse Oximeter.;Cough. Timepoint: In both groups, their intensity and grade were recorded at 0, 5 minutes, 10 minutes, 15 minutes and 2 hours after extubation. Method of measurement: Cough as: 0 No cough, 1 Brief cough, 2 Moderate cough, 3 Severe cough.;Laryngospasm. Timepoint: In both groups, their intensity and grade were recorded at 0, 5 minutes, 10 minutes, 15 minutes and 2 hours after extubation. Method of measurement: This observation is how to measure this variable.

Secondary

MeasureTime frame
Duration of extubation after drug closure. Timepoint: At the end of the study. Method of measurement: calculation.;The duration of return after reverse injection. Timepoint: At the end of the study. Method of measurement: calculation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAbulqasim Yousefi

Tehran University of Medical Sciences

Yousefi@sina.tums.ac.ir+98 21 6672 7061

Outcome results

None listed

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