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Study on uterine fibroid with vitamin D and prolactin.

Clinical study to assess the association of vitamin D and prolactin with uterine fibroid in premenopausal women - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/09/045404
Enrollment
200
Registered
2022-09-12
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: - Health Condition 2: O262- Pregnancy care for patient with recurrent pregnancy loss

Interventions

None listed

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria for case: 1.Female subjects with 18 to 50 years of age (both inclusive) who are in pre-menopausal status. 2.Documented evidence of atleast one uterine fibroid lesion of 2 cm3 or greater on ultrasonography. 3.Willing to participate in the study. Inclusion criteria for control: 1.Female subjects with 18 to 50 years of age (both inclusive) who are in pre-menopausal status. 2.Documented evidence of no uterine fibroid lesion on ultrasonography. 3.Willing to participate in the study.

Exclusion criteria

Exclusion criteria: Exclusion criteria for both cases and controls: 1.Pregnant and lactating women. 2.Women with a history of abortion or miscarriage in the last 6 months. 3.Women with a history of prior surgery for fibroids (myomectomy) or hysterectomy. 4.Women with concomitant use of vitamin D supplements or history of vitamin D supplement within the last 3 months. 5.Women with concomitant use of hormonal treatment (including oral contraceptives) or history of hormonal treatment within the last 3 months. 6.Women with concomitant use of drug known to increase the serum prolactin levels [e.g., haloperidol, chlorpromazine, thioridazine, thiothixene (typical antipsychotics); risperidone, amisulpride, molindone, zotepine (atypical antipsychotics); sertraline, fluoxetine, paroxetine, pargyline, clorgyline (antidepressants); buspirone, alprazolam (psychotropics); metoclopramide and domperidone (prokinetics), alpha-methyldopa, reserpine and verapamil (antihypertensive), morphine (opiates)]. 7.Women with diabetes mellitus, pituitary, and hypothyroidism, chronic renal failure, or psychiatric disease

Design outcomes

Primary

MeasureTime frame
The association of serum levels of Vitamin D3 and Prolactin will be evaluated in Patients with uterine fibroids and it will compare with healthy individuals.Timepoint: 12 Weeks

Secondary

MeasureTime frame
The association of serum levels of Vitamin D3 and Prolactin will be evaluated with number and size of uterine fibroids.Timepoint: 20 Weeks

Countries

India

Contacts

Public ContactAzaz Ahmad

Indira IVF Hospital Pvt. Ltd.

drnihar.bhoi@indiraivf.in7205783512

Outcome results

None listed

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