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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03991078
Other study ID # IIS-COL-2018-01
Secondary ID 1812-FIVI-100-AP
Status Recruiting
Phase
First received
Last updated
Start date July 9, 2019
Est. completion date December 25, 2024

Study information

Verified date February 2024
Source Fundación IVI
Contact Hortensia Ferrero, phD
Phone +34963903305
Email Hortensia.Ferrero@ivirma.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Vitamin D supplementation in patients with uterine fibroids who present hypovitaminosis D to re-establish their normal serum values could stabilize the size of the uterine fibroids and thus prevent their growth or reduce their size thanks to the anti-proliferative action of Vitamin D on the myoma cells.


Recruitment information / eligibility

Status Recruiting
Enrollment 15
Est. completion date December 25, 2024
Est. primary completion date December 25, 2024
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Diagnosed with at least one fibroid > 3 cm - With hypovitaminosis D (25(OH)D < 30 ng/ml) - BMI < 30 - No hormonal treatment in the 3 months prior to the ultrasound study Exclusion Criteria: - Black race - Symptomatic fibroids subsidiary to hormonal or surgical treatment - Desire of gestation in the next 6 months - Presence of degenerating adenomyosis or fibroids - Treatment with sexual hormones: mifepristone, aGnRH or any other medication that may interfere with fibroids. - History of neoplasia of gynecological origin and/or existence of uterine malformations. - Hypercalcemia or abnormal liver or kidney function is present

Study Design


Locations

Country Name City State
Spain Fundacion IVI Valencia

Sponsors (2)

Lead Sponsor Collaborator
Fundación IVI Hospital Universitario La Fe

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary volume of the uterine fibroids 3 months