- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07447011
Glaucoma Respsosne to Lifestyle Corrections in Sleep Apnea
February 26, 2026 updated by: Ali Mohamed Ali ismail, Cairo University
glaucoma is prevalent among obstructive sleep apnea (OSA).
contnous passive airway pressure is main treatment of OSA.
lifestyle corrections also recommended
Study Overview
Status
Recruiting
Intervention / Treatment
Detailed Description
forty glaucoma patients (high tension priamry open angle form) with OSA, intraocular pressure more than 21 mmHg, and obesity will be involved and divided to group I or group II (number of patients will be twenty in every group) for three month.
both groups will apply CPAP during night sleeping daily for three month.
group I will apply lifestyle corrections (low calories diet intake and 3-session per-week 40-minute treadmill walking for three month.
Study Type
Interventional
Enrollment (Estimated)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ali MA Ismail, lecturer
- Phone Number: 01005154209
- Email: ali.mohamed@pt.cu.edu.eg
Study Contact Backup
- Name: ali mohamed, lecturer
- Phone Number: 0201031321109
- Email: fatmaraed1994@gmail.com
Study Locations
-
-
Dokki
-
Giza, Dokki, Egypt
- Recruiting
- Cairo university
-
Contact:
- ali ismail, lecturer
- Phone Number: 02 01005154209
- Email: ali.mohamed@pt.cu.edu.eg
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Obstructive sleep apnea patients
- obese patients
- glaucoma (open angle form with ocular hyoertension)
Exclusion Criteria:
cardiac patients renal patients hepatic patients
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: group number 1
twenty glaucoma patients (high tension priamry open angle form) with OSA, intraocular pressure more than 21 mmHg, and obesity will be involved in group I will apply CPAP during night sleeping daily for three month.
group I will apply lifestyle corrections (low calories diet intake and 3-session per-week 40-minute treadmill walking for three month.
|
twenty glaucoma patients (high tension priamry open angle form) with OSA, intraocular pressure more than 21 mmHg, and obesity will be involved in group I will apply CPAP during night sleeping daily for three month.
group I will apply lifestyle corrections (low calories diet intake and 3-session per-week 40-minute treadmill walking for three month.
|
|
Active Comparator: group number 2
twenty glaucoma patients (high tension priamry open angle form) with OSA, intraocular pressure more than 21 mmHg, and obesity will be involved in group II will apply CPAP during night sleeping daily for three month.
|
twenty glaucoma patients (high tension priamry open angle form) with OSA, intraocular pressure more than 21 mmHg, and obesity will be involved in group II will apply CPAP during night sleeping daily for three month.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Intraocular pressure
Time Frame: it will be measured after 12 weeks
|
it will be measured by tonometery
|
it will be measured after 12 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
apnea hypopnea index
Time Frame: It will be measured after 12 weeks
|
it is an indicator on numbe rof apnea during sleep
|
It will be measured after 12 weeks
|
|
Epowrth sleepiness scale
Time Frame: It will be measured after 12 weeks
|
a questioanire assess rate of sleepiness
|
It will be measured after 12 weeks
|
|
body mass index
Time Frame: It will be measured after 12 weeks
|
it assesed on empty bladder and bowel
|
It will be measured after 12 weeks
|
|
waist circumference
Time Frame: it will be measured after 12 weeks
|
it will be assesed at umbilical level
|
it will be measured after 12 weeks
|
|
neck circumferfence
Time Frame: It will be measured after 12 weeks
|
it is a measures of local fat around neck
|
It will be measured after 12 weeks
|
|
glaucoma related quality of life questioanire
Time Frame: It will be measured after 12 weeks
|
it is 15-item questioanire assessing life quality in qlaucoma
|
It will be measured after 12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ali MA Ismail, lecturer, Cairo university
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 4, 2026
Primary Completion (Estimated)
July 20, 2026
Study Completion (Estimated)
July 20, 2026
Study Registration Dates
First Submitted
February 26, 2026
First Submitted That Met QC Criteria
February 26, 2026
First Posted (Actual)
March 3, 2026
Study Record Updates
Last Update Posted (Actual)
March 3, 2026
Last Update Submitted That Met QC Criteria
February 26, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Nervous System Diseases
- Nutrition Disorders
- Overnutrition
- Body Weight
- Respiratory Tract Diseases
- Respiration Disorders
- Eye Diseases
- Sleep Wake Disorders
- Overweight
- Apnea
- Sleep Disorders, Intrinsic
- Dyssomnias
- Sleep Apnea Syndromes
- Ocular Hypertension
- Glaucoma
- Pathological Conditions, Signs and Symptoms
- Nutritional and Metabolic Diseases
- Signs and Symptoms
- Obesity
- Sleep Apnea, Obstructive
- Glaucoma, Open-Angle
Other Study ID Numbers
- IRB000-14233-70
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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