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Investigating the effect of amino selenium in the treatment of endometriosis

The effect of supplementation with Amino selenium on the course of the disease, painful signs and symptoms in women with endometriosis: A triple blind randomized controlled trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110606006709N26
Enrollment
66
Registered
2023-12-30
Start date
2024-01-19
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Endometriosis. Endometriosis

Interventions

Intervention 1: Intervention group: A 250 mg capsule containing 200 µg of amino selenium enriched with Saccharomyces cerevisiae yeast was made at the Tabriz Nutrition Research Center and will be used

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Women of reproductive age (15-49 years) Being literate in reading and writing Women with primary endometriosis with endometrioma less than 5 cm Women with symptomatic endometriosis (dysmenorrhoea pain score of 16 or more in the Mous Menstrual Distress Questionnaire) Married women who are sexually active

Exclusion criteria

Exclusion criteria: Probability of malignancy based on vaginal ultrasound Definite need for surgery based on the opinion of obstetrician and gynecologist Suffering from diseases such as myoma or hyperplasia or polycystic ovary syndrome based on vaginal ultrasound Daily and regular consumption of supplements containing Amino Selenium during the last three months according to the patient's statement Suffering from liver and kidney diseases and the need for dialysis Pregnancy and breastfeeding Desire to get pregnant in the next trimester Allergy to Gelofen

Design outcomes

Primary

MeasureTime frame
Average endometrioma cyst size. Timepoint: Before the intervention and 3 months after the start of intervention. Method of measurement: Vaginal ultrasound.;Average dysmenorrhea score. Timepoint: Monthly during 3 months (1, 2, 3 months) after the start of the intervention. Method of measurement: Mous Menstrual Distress Questionnaire (MMDQ).

Secondary

MeasureTime frame
Average dyspareunia score. Timepoint: Monthly during 3 months (1, 2, 3 months) after the start of the intervention. Method of measurement: Visual analog scale (VAS).;Average score of dysuria. Timepoint: Monthly during 3 months (1, 2, 3 months) after the start of the intervention. Method of measurement: Visual analog scale (VAS).;Average score of Dyschezia. Timepoint: Monthly during 3 months (1, 2, 3 months) after the start of the intervention. Method of measurement: Visual analog scale (VAS).;Average score of non cyclic pain. Timepoint: Monthly during 3 months (1, 2, 3 months) after the start of the intervention. Method of measurement: Visual analog scale (VAS).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Teihoomanesh fard

Tabriz University of Medical Sciences

ftmf.97@gmail.com+98 41 3475 3906

Outcome results

None listed

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