Skip to content

Evaluation of the effect of herbal combination of fenugreek seeds and carrot seeds on sexual function 0fwomen with diabetes type 2,a randomized double-blinded clinical trial

Evaluation of the effect of herbal combination of fenugreek seeds and carrot seeds on sexual function of women with diabetes type 2,a randomized double-blinded clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210222050457N2
Enrollment
100
Registered
2023-05-08
Start date
2023-05-31
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Type 2 diabetes with sexual dysfunction?. Type 2 diabetes mellitus with unspecified complications

Interventions

Intervention 1: The intervention group consumes 500 mg herbal tablets three times a day. The drug is prescribed to patients for 8 weeks by a non-researcher, based on masking. The raw materials of this

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 55 Years

Inclusion criteria

Inclusion criteria: Married women with type 2 diabetes and sexual dysfunction HBA1C between 7.1 & 8.53. Age between 25 & 55 years diabetic patients should not have systemic diseases such as liver failure, kidney failure, heart failure, thyroid failure, central nervous system disorders, or retinopathy. Absence of pregnancy and breastfeeding Absence of Ovariectomy history and Ovarian agenesis Having a stable life with his wife Married for at least one year

Exclusion criteria

Exclusion criteria: Diagnosis of having chronic diseases affecting sexual function in the patient or his partner during the study (such as cardiovascular or mental or thyroid disorders, cancers) taking drugs that affect sexual performance The occurrence of an unfortunate incident such as the loss of partner or close relative during the study vaginal bleeding, dyspareunia, vaginismus Getting pregnant Menopause

Design outcomes

Primary

MeasureTime frame
Sexual function. Timepoint: At the beginning of the study and after two months of taking the drug. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
FBS. Timepoint: At the beginning of the study and 60 days after starting to take the drug. Method of measurement: Lab test.;2 hours post prandial blood sugar. Timepoint: At the beginning of the study and 60 days after starting to take the drug. Method of measurement: Lab test.;HB A1C. Timepoint: At the beginning of the study and 60 days after starting to take the drug. Method of measurement: Lab test.;Mental health. Timepoint: At the beginning of the study and 60 days after starting to take the drug. Method of measurement: questionare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh shirvanizadeh Arani

Yazd University of Medical Sciences

dr.shirvanizade@gmail.com+98 31 5472 5800

Outcome results

None listed

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