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Influence of Propofol on Alveolar Macrophage in Asthmatic Patients

Influence of Propofol on Alveolar Macrophage Immunity in Asthmatic Patients Undergoing General Anesthesia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00676416
Acronym
PAMAP
Enrollment
80
Registered
2008-05-13
Start date
2008-04-30
Completion date
2009-03-31
Last updated
2009-03-31

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

Conditions

Asthma

Keywords

General anesthesia, Propofol, Immunity, Alveolar Macrophages

Brief summary

The change of airway responsiveness and alveolar macrophage (AM) immunity occurs during the pathogenesis of asthma. Macrophage-associated airway protection in patients with asthma is affected positively or negatively by propofol general anesthesia. The investigators hypothesized that the effects of propofol on asthmatic AMs and corresponding airway reactivity in vivo is different from the in vitro research. Through in vivo airway hyperresponsiveness (AHR) observation and clinical investigation of AM immune functions from asthma patients undergoing propofol general anesthesia to clarify the precise effects of propofol on AM immunity, and to provide theoretical basis for the clinical administration of propofol in asthmatic patients. This would optimize the practice of clinical anesthesia, especially for those with the tendency of AHR.

Interventions

Propofol general anesthesia was performed in patients with asthma (1) and without asthma (2)

Sponsors

HRSA/Maternal and Child Health Bureau
CollaboratorFED
Nanjing Medical University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* ASA physical status I-II; * Aged from 18 years to 45 years; * Patients with or without asthma or a history record of asthma; * Undergoing elective lumpectomy under general anesthesia.

Exclusion criteria

* Allergy to propofol and opioids, a history of the use of centrally-acting drugs of any sort, chronic pain and psychiatric diseases records; * Participants younger than 18yr,older than 45yr or pregnancy; * Those who were not willing to or could not finish the whole study at any time; * The PACU assessing score was under 6 on a scale of 10 (measuring somnolence, respiration, movement, color, and blood pressure on 0-2 scales), and arterial oxygen saturation measured by pulse oximetry (SaO2) was 92% or lower (supplemental oxygen was permitted).

Design outcomes

Primary

MeasureTime frame
Alveolar macrophage viability assayOne day prior to the surgery, immediately after anaesthesia, at the beginning and the end of the operation and one day after surgeries.

Secondary

MeasureTime frame
Alveolar macrophage phagocytosis AssayOne day prior to the surgery, immediately after anaesthesia, at the beginning and the end of the operation and one day after surgeries.
Alveolar macrophage cytokine AssayOne day before the surgery, immediately after anaesthesia, at the beginning and the end of the operation and one day after surgeries.
Mean airway pressureBefore operation to the end of the surgery.
Curve shape of CO2Before operation to the end of the surgery.
End-tidal CO2Before operation to the end of the surgery.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026