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A study on the effect of ointment of pistacia atlantica oil on the prevention of stretch marks in primigravid wemon

A study on the effect of ointment of pistacia atlantica oil on the prevention of stretch marks in primigravid wemon

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230720058860N1
Enrollment
140
Registered
2023-11-27
Start date
2023-10-07
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

stretch marks. Diseases of the skin and subcutaneous tissue complicating pregnancy, childbirth and the puerperium.

Interventions

Intervention 1: Intervention group: The intervention process in the intervention group is such that on the first day of the research units' visit to the research environment, the researcher uses some

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Informed consent to participate in the study Age between 20 and 35 years Being pregnant for the first time Pregnancy age between 22 and 26 weeks Singleton pregnancy Not using corticosteroids and any type of topical or systemic corticosteroids Not using any kind of cream or oil in the abdominal area Not suffering from hydramnios Body mass index at the beginning of pregnancy or in the last trimester of the first trimester should be between 18.50 and 30 Mother's absence of Cushing's disease The absence of the mother from Marfan's disease The absence of the mother from anorexia nervosa The absence of the mother from chronic liver disease The absence of any type of lesion or wound at the intervention site Not having diabetes No allergy to Beneh ointment or no history of allergy to Beneh fruit

Exclusion criteria

Exclusion criteria: Reluctance to continue cooperation with the research unit Occurrence of hydramnios. Use of corticosteroid drugs (local and systematic). Use of any type of cream or oil on the abdominal area during the study Non-consecutive days during the study Rupture of fetal membranes, childbirth or termination of pregnancy for any reason Having gestational diabetes during the study

Design outcomes

Primary

MeasureTime frame
Itching. Timepoint: First day of visit and the day after the end of the intervention. Method of measurement: Kamini checklist.;Erythema. Timepoint: First day of visit and the day after the end of the intervention. Method of measurement: Otwal checklist.;Striae. Timepoint: First day of visit and the day after the end of the intervention. Method of measurement: Davey checklist.

Secondary

MeasureTime frame
Complication of the intervention. Timepoint: the day after the end of the intervention. Method of measurement: Copmlications checklist.;Satisfaction with the intervention. Timepoint: the day after the end of the intervention. Method of measurement: Intervention satisfaction questionnare.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Kobra Mirzaei

Mashhad University of Medical Sciences

Mirzakhanik@mums.ac.ir+98 938 420 2290

Outcome results

None listed

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