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Effects of Lactovag in treatment of vaginal dryness in Endometriosis

Effects of Lactovag on Treatment of Vaginal Dryness in Endometriosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180404039187N13
Enrollment
50
Registered
2025-04-19
Start date
2025-06-05
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Condition 1: Vaginal dryness and menopausal symptoms in endometriosis patients related to treatments used in endometriosis. Condition 2: Vaginal dryness and menopausal symptoms in endometriosis patients related to treatments used in endometriosis. Endometriosis Menopausal and female climacteric states

Interventions

Intervention 1: Intervention group: This group consists of 25 endometriosis patients with symptoms of vaginal dryness who will use the probiotic LactoVage vaginally for 14 days, one capsule daily. Lac

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients undergoing endometriosis treatment who suffer from the side effects of medications, including vaginal dryness. Patients who, according to the gynecologist's diagnosis, do not have an indication to receive conjugated estrogens. Patients with mild symptoms of vaginal dryness

Exclusion criteria

Exclusion criteria: Patients with severe symptoms of vaginal dryness that require conjugated estrogen. Patients who, according to the diagnosis of a gynecologist, have indications for surgery. Patients who suffer from other menstrual disorders in addition to endometriosis.

Design outcomes

Primary

MeasureTime frame
Vaginal dryness. Timepoint: 14 days after taking Lactovag. Method of measurement: Clinical examination by a gynecologist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElnaz Shaseb

Tabriz University of Medical Sciences

elnaz_shaseb_64@yahoo.com+98 41 3335 5921

Outcome results

None listed

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