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Comparative study of fibroptic bronchoscopic with two method: midazolam base versus lidocaine base

Comparative study of fibroptic bronchoscopic with two method: midazolam base versus lidocaine base in patients refered at lung clinic in AJA 501 hospital

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110103005536N8
Enrollment
140
Registered
2020-09-11
Start date
2019-05-22
Completion date
Unknown
Last updated
2020-10-06

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

Conditions

bronchoscopy.

Interventions

Intervention 1: Intervention group: In one group, for performing fibropeptic bronchoscopy, the method of anesthesia is used based on "midazolam". It is administered intravenously and after the fibropt

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: male and female patients aged 18 to 80 years ASA I-II

Exclusion criteria

Exclusion criteria: People with a history of sore throat and lung disease with 90% o2sat (hypoxemia) People with Ejection fraction less than 40% people with hearth rate less than 50 people with hypotension less than 90 mmHg People with III and grade II conduction blocks People with liver failure (2-fold increase in liver enzymes) and kidney failure (creatinine more than 2 mg / dL) Pregnant or lactating women People With a history of long-term use of antipsychotic drugs or sedatives.

Design outcomes

Primary

MeasureTime frame
Type of basic anesthetic. Timepoint: Before the intervention. Method of measurement: Based on the name of the drug.

Secondary

MeasureTime frame
Complications of bronchoscopy. Timepoint: During the intervention. Method of measurement: Based on the need for intubation, nausea, decreased oxygen saturation, sore throat, cough.;Duration of bronchoscopy. Timepoint: During the intervention. Method of measurement: Based on time from start to end of the procedure.;Physician satisfaction. Timepoint: After the intervention. Method of measurement: Based on the doctor's satisfaction with the procedure from 1 to 5 based on likret scale.;Patient satisfaction. Timepoint: After the intervention. Method of measurement: Based on the patient's satisfaction with the procedure from 1 to 5 based on likret scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Mohammadreza Rafiei

Artesh University of Medical Sciences

mo_rafiei@armyums.ac.ir+98 31 3261 6302

Outcome results

None listed

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