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Comparison between oral and nebulized Acetylcysteine in treatment of exacerbation of Chronic Obstructive Pulmonary Disease

Comparison between oral and nebulized Acetylcysteine in treatment of exacerbation of Chronic Obstructive Pulmonary Disease

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
PACTR
Registry ID
PACTR202508881358775
Enrollment
132
Registered
2025-08-21
Start date
2024-02-05
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Respiratory

Interventions

Standard treatment
Nebulized Acetylcysteine

Sponsors

Nadda
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult patients of both genders admitted in the ward with exacerbation of COPD (moderate exacerbation according to GOLD 2023). 2. Dyspnea with history of baseline dyspnea, expectoration or exposure to biomass fuel exposure or any similar occupational hazards. 3. Current smokers.

Exclusion criteria

Exclusion criteria: 1. Concomitant respiratory disease (e.g., asthma) or associated with a terminal disease (e.g., metastatic cancer). 2. Patients who need intensive care unit (ICU) admission and/or mechanical ventilation. 3. Patients who had taken any mucolytics in the preceding week. 4. Patients with gastro-intestinal bleeding or with risk of bleeding. 5. Pregnant women or breast-feeding mothers.

Design outcomes

Primary

MeasureTime frame
Improvement in the patient’s oxygen status with a target of saturation 88-92%.

Secondary

MeasureTime frame
Improvement in clinical status including dyspnea (applying Modified Medical Research Council (mMRC) dyspnea scale), wheezing (presented as percentage of patients), and decrease in time of stay in hospital (period of the exacerbation).

Countries

Egypt

Contacts

Public ContactNadda Badran

Study Coordinator Clinical Pharmacist Ain Shams Universities Hospital

naddagaber@gmail.com01110695887

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026