- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01622257
Cavitation Ultrasound in Treatment of Patients With PCOS
Comparison of Cavitation Ultrasound, Metformin or the Combination of Both in Obese Women With Polycystic Ovary Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Phase 2
Contacts and Locations
Study Locations
-
-
-
Cairo, Egypt
- Ain shams university
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Obese infertile polycystic ovarian syndrome (PCOS) women
Exclusion Criteria:
- Women 40 years or older
- Women using fertility treatments, oral contraceptives or other confounding medications during the last 3 months
- Smokers or with history of general diseases like cardiovascular, liver, kidney or respiratory disease, diabetes, uncontrolled hypertension, or malignancy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Cavitation US
Cavitation ultrasound was done using ultrasonic cavitation machine 2 times per week for 3 months
|
The areas with localized fat are treated 2 times per week for 3 months using Aesthetic cavitation via ultrasonic cavitation machine (Cavi SMART, South Korea, supplied with one piece cavitation probe of 40 KHz, 3-6 watt(W)/cm^2 adjustable, 60W with 20cm^2 active surface).
Other Names:
|
|
Experimental: Metformin
Metformin oral tablets 500 mg were given three times daily
|
Metformin hydrochloride (Glucophage 500 mg/tablet, Bristol-Myers Squibb, New York, USA).
Medication is initiated in a step-up fashion every 5 days, from one tablet per day to three.
This dose is maintained as tolerated throughout the 3 months of the study.
Other Names:
|
|
Experimental: Cavitation US + metformin
Combination of both Cavitation US + Metformin
|
Combination of both Cavitation US + Metformin.
the treatment duration lasts 3 months
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Clinical Pregnancy Rate
Time Frame: 9 months
|
9 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ovulation Rate as Determined by Ultrasonographic Folliculometry and Luteal Serum Progesterone Assay.
Time Frame: 3 months
|
The Number of participants who had evidence of successful ovulation during the 3 months. Ovulation was diagnosed based on ultrasonographic folliculometry and/or luteal serum progesterone assay.Every month, folliculometry was done to count the number of antral follicles (AFC), follow follicular growth, measure dominant follicle diameter and detect occurrence of ovulation. a mid-luteal serum progesterone assay was done to confirm ovulation. Ultrasound was performed serially till reaching preovulatory follicle(s of around 20 mm in diameter that then rupture to show a collapsed follicle in the same location with internal echoes consistent with its transformation to a corpus luteum. Progesterone assay was done using immulite 2000 apparatus chemiluminescent immunometric assay. Mid-luteal phase progesterone above 6 ng/mL was considered indicative of normal corpus. luteum function. |
3 months
|
|
Change in Insulin Resistance
Time Frame: Baseline and 3 months
|
Change in Fasting insulin concentration
|
Baseline and 3 months
|
|
Change in Serum Free Testosterone Level
Time Frame: Baseline and 3 months
|
Change in serum free testosterone levels
|
Baseline and 3 months
|
|
Change in Lipid Profile
Time Frame: Baseline and 3 months
|
Change in LDL levels was taken as the indicator of change in lipid profile
|
Baseline and 3 months
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Mostafa I. Ibrahem, M.D., Ain shams university
- Study Chair: Mohamed I. Ellaithy, MD, Lecturer Obstetics & Gynecology Ain shams university faculty of medicine
- Principal Investigator: Ahmed K. Makled, MD, Assistant professor of Obstetrics & Gynecology Ain shams university faculty of medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ASU6-2011
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.
Clinical Trials on PCOS
-
University Of PerugiaRecruiting
-
AdventHealth Translational Research InstituteActive, not recruiting
-
Guangdong Women and Children HospitalCompleted
-
Khyber Medical University PeshawarCompleted
-
Ain Shams Maternity HospitalUnknown
-
Mst.Sumyara KhatunBangladesh Medical UniversityRecruiting
-
Reproductive & Genetic Hospital of CITIC-XiangyaRecruiting
-
Mst.Sumyara KhatunCompleted
-
Amina AltutunjiHuazhong University of Science and TechnologyCompleted
Clinical Trials on Cavitation US
-
Cairo UniversityNot yet recruiting
-
Cairo UniversityAvailable
-
Cairo UniversityRecruiting
-
Cairo UniversityActive, not recruiting
-
Hasselt UniversityTerminated
-
University of VirginiaRecruiting
-
Riphah International UniversityCompleted
-
Cairo UniversityNot yet recruitingHealthy Adult Women
-
The Affiliated Hospital of Qingdao UniversityCompletedLung Cancer | Gastric Cancer Metastatic to Lung
-
Cairo UniversityCompleted