Improved Effects of MI Plus Alpha-LA in PCOS
Primary Purpose
Polycystic Ovary Syndrome
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
myo-inositol plus folic acid
myo-inositol plus folic acid plus alpha-lactalbumin
Sponsored by
About this trial
This is an interventional treatment trial for Polycystic Ovary Syndrome focused on measuring myo-inositol, alpha-lactalbumin, anovulation, infertility
Eligibility Criteria
Inclusion Criteria:
- patients affected by PCOS according to Rotterdam ESHRE-ASRM criteria, with anovulation and infertility > 1 year
Exclusion Criteria:
- presence of other conditions causing ovulatory dysfunction, such as hyperprolactinemia or hypothyroidism, or androgen excess, such as adrenal hyperplasia or Cushing's syndrome, and also in the case of intake of other drugs that can potentially influence the ovulation.
Sites / Locations
- Department of Woman Health and Reproductive Medicine of Santo Spirito Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Myo-inositol + folic acid
Myo-inositol + folic a. + α-lactalbumin
Arm Description
2 g myo-inositol and 0.2 mg folic acid orally twice a day for three months, in order to induce ovulation.
2 g myo-inositol and 0.2 mg folic acid plus 50 mg α-lactalbumin, twice a day for three months in order to test if α-lactalbumin addition allows to induce ovulation
Outcomes
Primary Outcome Measures
Restoration of ovulation
Ovulation was assessed using ultrasound examination on days 12, 14 and 20 of the cycle.
Secondary Outcome Measures
Increase of myo-inositol plasma levels after the treatment with myo-inositol plus alpha-lactalbumin compared to the levels at the baseline
Myo-inositol was dosed in plasma by means of gas chromatography-mass spectrometry
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03422289
Brief Title
Improved Effects of MI Plus Alpha-LA in PCOS
Official Title
Improved Effects of Myo-inositol in Association With Alpha-lactalbumin in PCOS Women
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
November 2, 2016 (Actual)
Primary Completion Date
October 12, 2017 (Actual)
Study Completion Date
December 15, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lo.Li.Pharma s.r.l
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
PCOS patients are initially treated with 2 g myo-inositol and 0.2 mg folic acid, two times per day by oral route, for three months. Among them, the subjects who have not ovulated despite this treatment are administered with 2g myo-inositol and 0.2 mg folic acid plus 50 mg α-lactalbumin for three months. Most of them improve and achieve ovulation. Therefore, the combination of α-lactalbumin with myo-inositol allows to get a significant result in the treatment of PCOS patients.
Detailed Description
Polycystic ovary syndrome is a complex chronic condition inducing several related disorders, such as subfertility and pregnancy complications. So far myo-inositol, successfully used in PCOS, has not been always effective in all patients. Aiming at overcoming this drawback, we tested a new formulation with myo-inositol and α-lactalbumin, in consideration of the effects exerted by α-lactalbumin in favoring molecule passage among body compartments, and also in consideration of its anti-inflammatory activity.
Only PCOS patients, according to Rotterdam ESHRE-ASRM criteria, with anovulation and infertility > 1 year, were included in the study. Following a treatment with 2 g myo-inositol and 0.2 mg folic acid, a part of them are resistant and do not ovulate.
These non-responders to myo-inositol alone undergo the second phase of the study, receiving 2g myo-inositol and 0.2 mg folic acid plus 50 mg α-lactalbumin for three months. After this combined treatment, the majority of them ovulate, showing a hormone and lipid profile improvement. In addition, myo-inositol plasma levels at the end of the treatment are significantly higher than at baseline and comparable to those patients who respond positively to myo-inositol alone.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Polycystic Ovary Syndrome
Keywords
myo-inositol, alpha-lactalbumin, anovulation, infertility
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Sequential Assignment
Model Description
All the patients were given orally Inofolic® (Lo.Li. Pharma, Rome, Italy), containing 2 g myo-inositol and 0.2 mg folic acid twice a day for three months, in order to induce ovulation. Then, non-responder partecipants were administered orally with 2 g myo-inositol plus 50 mg α-lactalbumin, twice a day for three months
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
37 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Myo-inositol + folic acid
Arm Type
Experimental
Arm Description
2 g myo-inositol and 0.2 mg folic acid orally twice a day for three months, in order to induce ovulation.
Arm Title
Myo-inositol + folic a. + α-lactalbumin
Arm Type
Experimental
Arm Description
2 g myo-inositol and 0.2 mg folic acid plus 50 mg α-lactalbumin, twice a day for three months in order to test if α-lactalbumin addition allows to induce ovulation
Intervention Type
Dietary Supplement
Intervention Name(s)
myo-inositol plus folic acid
Intervention Description
this treatment is made in the first phase of the study for three months
Intervention Type
Dietary Supplement
Intervention Name(s)
myo-inositol plus folic acid plus alpha-lactalbumin
Intervention Description
this treatment is made in the second phase of the study and it has a new molecule added to the previous ones administered in the first phase of the study
Primary Outcome Measure Information:
Title
Restoration of ovulation
Description
Ovulation was assessed using ultrasound examination on days 12, 14 and 20 of the cycle.
Time Frame
after three months of treatment
Secondary Outcome Measure Information:
Title
Increase of myo-inositol plasma levels after the treatment with myo-inositol plus alpha-lactalbumin compared to the levels at the baseline
Description
Myo-inositol was dosed in plasma by means of gas chromatography-mass spectrometry
Time Frame
after three months of treatment
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients affected by PCOS according to Rotterdam ESHRE-ASRM criteria, with anovulation and infertility > 1 year
Exclusion Criteria:
presence of other conditions causing ovulatory dysfunction, such as hyperprolactinemia or hypothyroidism, or androgen excess, such as adrenal hyperplasia or Cushing's syndrome, and also in the case of intake of other drugs that can potentially influence the ovulation.
Facility Information:
Facility Name
Department of Woman Health and Reproductive Medicine of Santo Spirito Hospital
City
Rome
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29747700
Citation
Montanino Oliva M, Buonomo G, Calcagno M, Unfer V. Effects of myo-inositol plus alpha-lactalbumin in myo-inositol-resistant PCOS women. J Ovarian Res. 2018 May 10;11(1):38. doi: 10.1186/s13048-018-0411-2.
Results Reference
derived
Learn more about this trial
Improved Effects of MI Plus Alpha-LA in PCOS
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