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Effect of chamomille oil massage for bronchiolitis

Comparison of chamomilla oil massage versus conventional treatment in bronchiolitis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20080930001285N1
Enrollment
60
Registered
2019-01-10
Start date
2016-09-22
Completion date
Unknown
Last updated
2019-01-29

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

Conditions

Bronchiolitis. Acute bronchiolitis, unspecified

Interventions

Intervention 1: Intervention group: In addition to the treatment of disease by ventolin nebulizer and supportive care (serum and suplimental oxygen therapy) such as control group, chamomile oil massag

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Months to 12 Months

Inclusion criteria

Inclusion criteria: first attack of bronchiolitis age between 1 to 12 months moderate to severe bronchiolitis

Exclusion criteria

Exclusion criteria: prematurity(birth age less than 37 weeks) history of bronchiolitis in past chronic heart and lung diseases immunodeficiency disease Down syndrome or others syndromic disease metabolic or neurological diseases The positive history of asthma in the first degree related

Design outcomes

Primary

MeasureTime frame
Changes in the percentage of venous oxygen saturation by pulse oximetry before and after treatment at intervals. Timepoint: before and 1 and 4 hour after treatment and then every 12 hours until discharging of patients. Method of measurement: pulse oximetry divise.;Heart rate changes. Timepoint: before and 1 and 4 hour after treatment and then every 12 hours until discharging of patients. Method of measurement: Awareness of heart rate and counting it in a minute,.;Changes in the number of breaths per minute. Timepoint: before and 1 and 4 hour after treatment and then every 12 hours until discharging of patients. Method of measurement: Listening to the respiratory sound and counting it in a minute.;Change in respiratory sounds. Timepoint: before and 1 and 4 hour after treatment and then every 12 hours until discharging of patients. Method of measurement: The sound of breathing sounds by stethoscope.;Pediatric Respiratory severity Score. Timepoint: before and 1 and 4 hour after treatment and then every 12 hours until discharging of patients. Method of measurement: Counting numbers.

Secondary

MeasureTime frame
The secondary outcome was the number of days admitted to the hospital. Timepoint: Until admission in the hospital. Method of measurement: counting the days of hospitalization.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Tahghighi

Yazd University of Medical Sciences

dr.tahghighi@gmail.com+98 35 3726 4677

Outcome results

None listed

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