Effect of Iranian Carrot Syrup (Parsnip) on Female Sexual Dysfunction

Investigation on the Effect of Iranian Carrot Syrup (Parsnip) on Female Sexual Dysfunction: A Triple Blind Clinical Trial

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20161004030131N2

Enrollment

Registered

2019-04-28

Start date

2019-05-14

Completion date

Unknown

Last updated

2019-05-21

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

Conditions

Sexual Dysfunction. Unspecified sexual dysfunction, not caused by organic disorder or disease

Interventions

Intervention 1: Intervention group: Iranian Carrot Syrup (Parsnip) is a combination of 7 Iranian Pastinaca sativa L,Pimpinella anisum , honey, Elettaria cardamomum, Crocus sativus(saffron), Dianthus

Eligibility

Sex/Gender

Female

Age

18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Sexual dysfunction in 6 independent areas ( desire, mental stimulation, lubrication, orgasm, satisfaction and pain) Age range 18 to 40 years Married Sexually active

Exclusion criteria

Exclusion criteria: Severe depression in the patient Pregnancy History of skin sensitivity to herbs in the family of Chattan Use of a drug affecting desire or sexual function such as serotonergic drugs (including citalopram fluoxetine, etc.) Consuming energy drinks and consuming Drugs Consuming blood diluent such as aspirin, warfarin, heparin or low molecular weight heparins Chronic diseases such as diabetes, hormonal disorders such as thyroid, prolactin Family problems and marital conflicts Rape history Wife's sexual problem Consumption Anti hypertensive drugs Menopause

Design outcomes

Primary

Measure	Time frame
Overall sexual performance score for women with sexual dysfunction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Female Sexual Function Index questionnaire.;Average score for each sexual function areas ( desire, mental stimulation, lubrication, orgasm, satisfaction and pain) in women with sexual dysfunction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Female Sexual Function Index questionnaire.;Depression. Timepoint: Before intervention. Method of measurement: Beck Depression Inventory questionnaire.	—

Measure

Time frame

Overall sexual performance score for women with sexual dysfunction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Female Sexual Function Index questionnaire.;Average score for each sexual function areas ( desire, mental stimulation, lubrication, orgasm, satisfaction and pain) in women with sexual dysfunction. Timepoint: Before intervention and 4 weeks after intervention. Method of measurement: Female Sexual Function Index questionnaire.;Depression. Timepoint: Before intervention. Method of measurement: Beck Depression Inventory questionnaire.

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Secondary

Measure	Time frame
-. Timepoint: -. Method of measurement: -.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Shabani

Arak University of Medical Sciences

f.shabani@arakmu.ac.ir+98 86 3417 3502

Outcome results

None listed

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