Role of Melatonin Supplementation in Follicular Fluid of in Vitro Fertilization (IVF) Patients With Polycystic Ovarian Syndrome

Sponsor
AGUNCO Obstetrics and Gynecology Centre (Other)
Overall Status
Completed
CT.gov ID
NCT01540747
Collaborator
(none)
1
2

Study Details

Study Description

Brief Summary

To evaluate the effects of melatonin supplementation on the main in vitro fertilization (IVF) outcomes during ovarian stimulation in patients with Polycystic ovarian syndrome (PCOS).

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Myo-inositol + folic acid + melatonin
  • Dietary Supplement: Myo-inositol + folic acid
Phase 4

Detailed Description

Polycystic ovarian syndrome (PCOS) is a common endocrine disorder that causes infertility due to anovulation in women of reproductive age. Anovulation and also decreased oocyte and embryo quality may be cause of infertility in women with PCOS. Furthermore, the reactive oxygen species (ROS) induce oxidative stress which may be responsible for poor oocyte quality. The ROS generation from mononuclear cells is elevated in women with PCOS and a significant increment of lipid peroxidation products in women with PCOS has been reported.

Melatonin is a documented powerful free radical scavenger and a broad spectrum antioxidant. It has been observed that a non-PCOS group co-treated with inositol, folic acid, and melatonin (Inofolic Plus by LO.LI.Pharma) results in a significantly greater mean number of mature oocytes, and a lower mean number of immature oocytes in patients with low oocyte quality history when compared to treatment only with inositol and folic acid (Inofolic by LO.LI.Pharma).

The aim of the study is to evaluate the possible effects of melatonin supplementation on the main IVF outcomes during ovarian stimulation of patients with PCOS.

From July 2009 to December 2011, 358 patients with PCOS (Rotterdam criteria) were enrolled in this prospective randomized controlled trial.

Study Design

Study Type:
Interventional

Arms and Interventions

Arm Intervention/Treatment
Experimental: Inofolic plus

178 patients

Dietary Supplement: Myo-inositol + folic acid + melatonin
Myo-inositol (2000mg)+ folic acid (200 mcg)+ melatonin(3 mg)

Active Comparator: Inofolic

180 patients

Dietary Supplement: Myo-inositol + folic acid
Myo-inositol (2000mg) + folic acid (200 mcg)

Outcome Measures

Primary Outcome Measures

  1. Number of mature oocytes []

  2. embryo quality []

  3. Pregnancy rate []

  4. Implantation rate []

Secondary Outcome Measures

  1. Total dose of FSH administered []

  2. Number of days of stimulation []

  3. Serum estradiol levels []

  4. Endometrial thickness []

    Endometrial thickness on the day of human chorionic gonadotropin (hCG) administration

  5. Cancellation rate []

  6. Incidence of moderate or severe ovaric hyperstimulation syndrome (OHSS) []

Eligibility Criteria

Criteria

Ages Eligible for Study:
27 Years to 38 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • diagnosis of PCOS

  • irregular menstrual cycle (> than 28-30 days)

  • normal uterine cavity

  • body mass index of 20 to 26 Kg/m2

  • first IVF treatment

Exclusion Criteria:
  • presence of tubal, uterine, genetics and male causes of infertility

  • diagnosis of cancer

  • hormonal treatment in the last six months

Contacts and Locations

Locations

Site City State Country Postal Code
1 Praxi Pro Vita Centro di Fertilità Rome Italy

Sponsors and Collaborators

  • AGUNCO Obstetrics and Gynecology Centre

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
AGUNCO Obstetrics and Gynecology Centre
ClinicalTrials.gov Identifier:
NCT01540747
Other Study ID Numbers:
  • Mel_FF
First Posted:
Feb 29, 2012
Last Update Posted:
Feb 29, 2012
Last Verified:
Jan 1, 2009
Keywords provided by AGUNCO Obstetrics and Gynecology Centre
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 29, 2012