stretch marks. Diseases of the skin and subcutaneous tissue complicating pregnancy, childbirth and the puerperium.
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time 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
| Measure | Time 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
Mashhad University of Medical Sciences