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D-chiro-inositol and Endometrial Thickness

L

Lo.Li.Pharma

Status

Completed

Conditions

Endometrial Diseases

Treatments

Dietary Supplement: DCI

Study type

Interventional

Funder types

Industry

Identifiers

NCT05283642
DCI_GYN22

Details and patient eligibility

About

Investigation of the effects of D-chiro-inositol supplementation in women with altered endometrial thickness.

Enrollment

13 patients

Sex

Female

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • altered endometrial thickness

Exclusion criteria

  • patients with cancer
  • patients under hormonal treatments (progestogens and/or estrogens)
  • patients supplemented with inositols

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

13 participants in 1 patient group

DCI
Experimental group
Description:
Oral supplementation with D-chiro-inositol once a day
Treatment:
Dietary Supplement: DCI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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