Ovarian Stimulation: Inositol and Melatonin

Sponsor
AGUNCO Obstetrics and Gynecology Centre (Other)
Overall Status
Unknown status
CT.gov ID
NCT01267604
Collaborator
University of Modena and Reggio Emilia (Other), Research Center for Reproductive Medicine Villa Mafalda (Other)
150
2
2
75

Study Details

Study Description

Brief Summary

An efficient protocol of ovarian stimulation is a key part of assisted reproductive technology. In order to obtain the highest oocyte retrieval with no adverse effects, numerous studies have evaluated the efficiency of the clinical approaches currently available.

Recent studies have shown that two natural compounds, such as inositol and melatonin, play an important role in oocyte maturation and quality. Therefore, the present study aims at investigating whether inositol and melatonin are able to improve the number of oocytes obtained after ovarian stimulation with Recombinant Follicle Stimulating Hormone (rFSH).

To this purpose, a randomized double-blind trial will be established where 150 healthy women in reproductive age undergoing to assistant reproductive technology (ART) because of male infertility will be divided in two groups. Group A will be treated with 225IU rFSH alone, group B will be treated with 225IU rFSH, 4g inositol and 3mg melatonin.

As primary outcome of the study, oocyte quality, total number of oocytes retrieved, clinical pregnancy rate and live birth rate will be evaluated in group A vs. group B.

Condition or Disease Intervention/Treatment Phase
  • Drug: Recombinant FSH (rFSH)
  • Dietary Supplement: rFSH + Inositol + Melatonin
Phase 4

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Improving Oocyte Retrieval Using a Combined Therapy of Recombinant Follicle Stimulating Hormone (rFSH) and Inositol and Melatonin
Study Start Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Recombinant FSH

225IU rFSH

Drug: Recombinant FSH (rFSH)
225IU

Experimental: Recombinant FSH Inositol Melatonin

225IU rFSH, 4g Inositol and 3mg Melatonin

Dietary Supplement: rFSH + Inositol + Melatonin
225IU rFSH, 4g Inositol, 3mg Melatonin

Outcome Measures

Primary Outcome Measures

  1. Total oocyte number [2 weeks after pharmacological treatment]

  2. Number of clinical pregnancies [6 weeks after embryo transfer]

  3. Live birth rate [10 months after embryo transfer]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 39 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Female age 18-39 years

  • BMI 18-30 kg/m2,

  • Fewer than 3 prior oocyte retrievals,

  • No fertility Problems

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Modena and Reggio Emilia Reggio Emilia Italy 42100
2 Research Center for Reproductive Medicine Villa Mafalda Roma Italy 00199

Sponsors and Collaborators

  • AGUNCO Obstetrics and Gynecology Centre
  • University of Modena and Reggio Emilia
  • Research Center for Reproductive Medicine Villa Mafalda

Investigators

  • Study Director: Vittorio Unfer, MD, AGUNCO Obstetrics and Gynecology Centre
  • Principal Investigator: Gianfranco Carlomagno, PhD, AGUNCO Obstetrics and Gynecology Centre
  • Principal Investigator: La Sala Giovanni Battista, MD, University of Modena and Reggio Emilia
  • Principal Investigator: Franco Lisi, MD, Research Center for Reproductive Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT01267604
Other Study ID Numbers:
  • rFSH-INOPLUS
First Posted:
Dec 28, 2010
Last Update Posted:
Dec 28, 2010
Last Verified:
Dec 1, 2010
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 28, 2010