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Effect of Hypocaloric Diet and Exercise in Obese Women Who Are Subjected to IVF Cycle

Effect of Hypocaloric Diet and Exercise in Obese Women Who Are Subjected to IVF Cycle

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01952795
Enrollment
41
Registered
2013-09-30
Start date
2013-11-30
Completion date
2016-04-30
Last updated
2017-08-22

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

Conditions

Obesity

Brief summary

The purpose of this study is to determine the impact of diet and physical exercise program on pregnancy rate and live birth in obese women who undergo an IVF cycle.

Detailed description

The objective of this study is showing that obesity significantly affects the in vitro fertilization cycles lowering the reproductive capacity. The study is been performed in Hospital de la Santa Creu i Sant Pau and Fundació Puigvert of Barcelona. Patients recluted are obese women with sterility problems that require in vitro fertilization (IVF) with a body mass index BMI between 30-35. It´s a randomised study in which half of the patients undergo to a 6 weeks program of diet and exercice. We will analyse the response to ovaric stimulation, the results of the egg retrieval (ovocyte number and quality), rates of fecundation, embryo implantation and clinical gestation.

Interventions

BEHAVIORALDiet and exercise

Total caloric intake aimed at maintaining a diet with\> 50% of the caloric content in the form of carbohydrates, less than 10% in the form of saturated fats and 20% from monounsaturated / polyunsaturated (if applicable, up to 25% fat monounsaturated), less than 300 mg / day of dietary cholesterol and about 1.0 g of protein / kg ideal body weight / day.

Sponsors

Fondo de Investigacion Sanitaria
CollaboratorOTHER
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Women who want pregnancy. * Basal FSH levels ≤ 10 IU / l. * Infertility to justify treatment with IVF/ICSI. * Being included in a long protocol with GnRH agonist. * Presence of both ovaries and uterus able to support embryo implantation and pregnancy. * Body mass index (BMI) ≥ 30 kg/m2 and ≤ 35 kg/m2. * Absence of pregnancy before starting ovarian stimulation. * Having given their written consent.

Exclusion criteria

* Female age ≤ 18 years and ≥ 35 years. * Severe male factor not permit an IVF-ICSI with ejaculated sample. * Patients with low ovarian reserve (basal FSH levels ≥ 10 IU / l or lower antral follicle count to 6 follicles in both ovaries). * HIV seropositivity, HBV or HCV. * Clinically important disease. * Having frozen embryos from previous cycles of assisted reproduction. * Unexplained vaginal bleeding. * Poor response in previous IVF cycles with standard stimulation protocols * Any contraindication to become pregnant. * Known allergy to preparations of gonadotropins or its excipients. * High consumption of alcohol, drugs or psychotropic drugs. * Concurrent participation in another study. * Patients who have done previous cycles of IVF / ICSI without success

Design outcomes

Primary

MeasureTime frameDescription
Pregnancy rate14 days after embryo transferPregnancy rate by cycle

Secondary

MeasureTime frameDescription
Hyperstimulation rateAt luteal phase and first weeks of pregnancyNumber of patients with moderate or severe hyperstimulation
Fertility rate24 hours post pick upRate of mature oocytes fertilized by conventional IVF or ICSI
Mature oocytesPick up dayNumber of total mature oocytes obtained after stimulation
Good quality embryosDay 3 to 5 post pick upNumber of good quality embryos obtained (A and B) by patient
Abortion rateFirst trimester of pregnancyNumber of non evolutive pregnancies during the first trimester
Live birth rateBetween 7 a 9 months after treatmentAmount of patients who finish the treatment with a live newborn
Cancellation rateDurinf the stimulation in follicular phaseStimulated Patients who fail to perform the follicular puncture

Other

MeasureTime frameDescription
Leptin, adiponectin, resistin, interleukin VI, TNF-α, visfatin, IGF1 and PAI IDuring the stimulation phaseStudy the relationship between obesity and measurable surrogate parameters the same as the products of secretion of fat (leptin, adiponectin, resistin, interleukin VI, TNF-α, visfatin, IGF1 and PAI I) or with inflammatory parameters results of an IVF cycle.

Countries

Spain

Outcome results

None listed

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