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Effect of Laser Puncture Versus Ultraviolet Radiation on Women With Polycystic Ovarian Syndrome

Effect of Laser Puncture Versus Ultraviolet Radiation on Women With Polycystic Ovarian Syndrome

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05986838
Enrollment
100
Registered
2023-08-14
Start date
2023-08-30
Completion date
2024-04-30
Last updated
2024-02-09

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

Conditions

Polycystic Ovary Syndrome

Brief summary

Obese women with polycystic ovarian syndrome aged between 25 and 35 years old will be divided into three groups. For three months, group (A) will receive laser puncture (3 sessions per week), along with a metformin supplementation, group (B) will receive ultraviolet radiation (3 sessions per week), along with a metformin supplementation, while group (C) will receive only metformin supplementation. The follicular size will be measured using ultrasound, while, female sex hormones, and serum 25-hydroxyvitamin D levels will bel evaluated using blood analysis

Detailed description

Obese women with polycystic ovarian syndrome aged between 25 and 35 years old will be divided into three groups. For three months, group (A) will receive laser puncture (3 sessions per week), along with a metformin supplementation, group (B) will receive ultraviolet radiation (3 sessions per week), along with a metformin supplementation, while group (C) will receive only metformin supplementation. The follicular size will be measured using ultrasound, while, female sex hormones, and serum 25-hydroxyvitamin D levels will bel evaluated using blood analysis

Interventions

DEVICEaser puncture

laser puncture (3 sessions per week)

DEVICEultraviolet radiatio

ultraviolet radiation (3 sessions per week)

DRUGMetformin

for 3 months

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Obese nulli gravid PCOS women * BMI 30-40 kg/m2

Exclusion criteria

* hyperprolactinemia * BMI \> 40 kg/m2 Endocrinological disorders such as thyroid disease, Cushing's syndrome, Coagulopathy * Recent use of oral contraceptive pills * Recent use of any photosensitizing medications, such as aspirin, tetracycline, chlorothiazide, or psoralen suspicious of neoplasms

Design outcomes

Primary

MeasureTime frameDescription
LH/FSH ratio1 month after treatmentLH/FSH ratio measured in venous sample on day 3 of the menstrual cycle

Secondary

MeasureTime frameDescription
Serum 25-hydroxyvitamin D concentration1 month after treatment25-hydroxyvitamin D measured in venous sample

Countries

Egypt

Contacts

Primary ContactAhmed M Maged
Ahmedmaged@cu.edu.eg+201005227404
Backup ContactWafaa Kamal
wafaa_kamal37@yahoo.com01006914119

Outcome results

None listed

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