Skip to content

The effect of vitamin D on quality of life and symptom severity of symptomatic uterine Leiomyoma in women

The effect of vitamin D on quality of life and symptom severity of symptomatic uterine Leiomyoma in women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160821029446N7
Enrollment
92
Registered
2020-04-04
Start date
2020-05-20
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

Uterine leiomyoma. Leiomyoma of uterus, unspecified

Interventions

Intervention 1: Intervention group: will receive 50,000 weekly dose of Pearl Vitamin D in addition to medical treatment of uterine leiomyoma for 8 weeks. Intervention 2: Control group: will receive a

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Age between 15-49 years At least existence of one confirmed uterine leiomyoma in the ultrasound without need of surgery Existence of uterine leiomyoma symptoms in history Under medical treatment of uterine leiomyoma 25 hydroxy vitamin D values less than 30 ng/ml

Exclusion criteria

Exclusion criteria: Pathology existence of the uterus, ovaries and adnexes in sonography Existence of contraindication for vitamin D intake Existence of any chronic medical condition Pregnancy or desire to become pregnant within the next 6 months and lactation

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Before, 2 and 4 months after intervention. Method of measurement: Uterine Fibroid Symptom & Health-Related Quality Of Life Questionnaire.;Uterine Fibroid Symptom. Timepoint: Before, 2 and 4 months after intervention. Method of measurement: Uterine Fibroid Symptom & Health-Related Quality Of Life Questionnaire.

Secondary

MeasureTime frame
Serum concentration of 25-hydroxy vitamin D3. Timepoint: Before and 4 months after intervention. Method of measurement: Elisa test.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSamira Noorzaie

Tehran University of Medical Sciences

snoorzaie1374@gmail.com+98 21 6692 7171

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026