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The Effect of rose damascene oil and sesame oil on the prevention of striae gravidarum

The Effect of rose damascene oil, sesame oil and placebo on the prevention of striae gravidarum in nulliparous women: A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20131009014957N9
Enrollment
150
Registered
2020-03-14
Start date
2020-06-14
Completion date
Unknown
Last updated
2020-03-24

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

Conditions

Pregnancy striae. Other disorders of skin and subcutaneous tissue in diseases classified elsewhere

Interventions

Intervention 1: Intervention group 1: Rose damascene oil. The 10% rose damascene oil at the base of the cream will be produced by a pharmacognosist at the Biotechnology Research Center and it will be

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Gestational age of 16-20 weeks Having a single live fetus Nulliparity Being at the age of 18-35 years Body mass index of 18.5-25 kg /m2 Being literate (at least writing and reading skills)

Exclusion criteria

Exclusion criteria: The use of other herbal or chemical drugs on the affected area Sensitivity to rose oil and sesame oil and not being able to use the drug twice daily Taking corticosteroids previous striae Surgical scar on the abdomen Having chronic diseases Having adrenal glands diseases Presence of skin disease

Design outcomes

Primary

MeasureTime frame
Incidence rate of gestational striae. Timepoint: Evaluation of incidence in 35-37 weeks of gestation. Method of measurement: Davey method.;Incidence rate of itching. Timepoint: The incidence of pruritus in 35-37 weeks of gestation. Method of measurement: Kamini method.;Severity of gestational striae. Timepoint: Evaluation of severity of striae in 35-37 weeks of gestation. Method of measurement: Davey method.;Severity of itching. Timepoint: Evaluation of severity of pruritus in 35-37 weeks of gestation. Method of measurement: Kamini method.

Secondary

MeasureTime frame
Satisfaction of medication use. Timepoint: 35-38 weeks of gestation. Method of measurement: Satisfaction Questionnaire.;Side effects. Timepoint: 35-38 weeks of gestation. Method of measurement: Side effects Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzizeh Farshbaf-khalili

Tabriz University of Medical Sciences

farshbafa@tbzmed.ac.ir+98 41 3335 2295

Outcome results

None listed

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