Finding studies
Finding studies
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Hieba Gamal Gamal Ezz El Regal, PhD
CONTACT
Lead
Cairo University
With
Study Design and Setting This study is a phase IV randomized controlled clinical trial (RCT) involving 60 adult patients diagnosed with asthma. Participants will be recruited from the outpatient clinic and pulmonary function unit of the Chest Department at Ain Shams University Hospitals. Study Type: Phase IV randomized controlled clinical trial (RCT) Study Setting: Outpatient clinic and pulmonary function unit, Chest Department, Ain Shams University Hospitals Study Population: Adult patients with asthma, obesity, and diabetes mellitus Sampling and Randomization Participants will be randomly assigned to study groups using computer-generated randomization sequences. Allocation concealment will be ensured through the use of sealed, opaque envelopes. Ethical Considerations The study protocol will be explained clearly to all eligible participants prior to enrollment. The study will commence only after obtaining approval from the Ethical Committee of the Faculty of Medicine, Ain Shams University. Written informed consent will be obtained from all participants prior to inclusion. Participant safety will be prioritized, and all efforts will be made to minimize potential risks. Confidentiality and anonymity of participant data will be strictly maintained. All participants will have an equal chance of being assigned to either study group. No deceptive practices will be used during the study. Participants will have the right to withdraw from the study at any time without any consequences. Study Procedures All eligible participants will undergo the following assessments: Demographic Data Collection: Age, sex, smoking status, and body mass index (BMI) Clinical Assessment: Detailed medical history including environmental exposures, potential risk factors, comorbidities, and duration of disease Concomitant Care All participants will continue receiving standard asthma therapy throughout the study period. Participants will be instructed to maintain a consistent intake of chromium-rich foods during the study to avoid dietary confounding.
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
