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The effect of dill vaginal cream on treatment of candida vaginitis

The comparision effect of Anethum graveolens L. (dill) products on traditional medicine base with clotrimazole cream 1% on vaginal candidiasis.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016071929004N1
Enrollment
105
Registered
2016-10-12
Start date
2016-07-14
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

vulvovaginal Candidiasis. Candidiasis of vulva and vagina

Interventions

Intervention 1: using one applicator of Essential oil of Anethum graveolens L. (Dill) vaginal cream (2%) every night for 7 nights. Intervention 2: using one applicator of Clotrimazole vaginal cream 1
Treatment - Drugs
using one applicator of Essential oil of Anethum graveolens L. (Dill) vaginal cream (2%) every night for 7 nights.
using one applicator of Clotrimazole vaginal cream 1% every night for 7 nights .
using one applicator of total extract of dill vaginal cream (2%) every night for 7 nights .

Sponsors

Vice chancellor for research, Kerman University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: sign and symptoms of vulvovaginal candidiasis; married women; between 18 to 65 years old; with positive sniff test; without pregnancy, without breast feeding, without chronic disease such as (kidney ,liver, cardiac disease and diabetes ), no existance of immunodeficiency nor complicated vaginal candidiasis on diagnosis of gynecologist and not using of systemic antibiotics and immunosuppressive drugs, or any vaginal drugs during the study and not using of systemic anti fungal drugs since 4 weeks ago. Exclusion criteria: side effects or drug reaction; pregnancy; menstruate; lack of patient's association.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Burning. Timepoint: at the beginning and 10 days after intervention. Method of measurement: Evaluation of clinical symptom's remission(burning) with VSQ (vulvovaginal symptom questionnaire).;Itching. Timepoint: at the beginning and 10 days after intervention. Method of measurement: Evauation of clinical symptom's remission (itching) with VSQ (vulvovaginal symptom questionnaire).;Vaginal discharge. Timepoint: at the beginning and 10 days after intervention. Method of measurement: Evaluation of clinical symptom's remission (vaginal discharge) with VSQ (vulvovaginal symptom questionnaire).;Erithema. Timepoint: at the beginning and 10 days after intervention. Method of measurement: physical exam.;Edema. Timepoint: at the beginning and 10 days after intervention. Method of measurement: physical exam.

Secondary

MeasureTime frame
Sniff test outcome. Timepoint: at the beginning and 10 days after intervention. Method of measurement: vaginal smear.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZohreh Sarhadinejhad

Kerman University Of Medical Sciences

z_sarhadinejhad@kmu.ac.ir; dr_isac1390@ yahoo.com00983433122020; 00983433122023; 00983431325720

Outcome results

None listed

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