Striae gravidarum. Pregnancy, childbirth and the puerperium
Conditions
Interventions
Intervention 1: The first intervention group will recieved 1 cc sesame oil twice a day during 20 weeks. Intervention 2: The second intervention group will received 1 cc sweet almond oil ,twice a day
Prevention
Placebo
The first intervention group will recieved 1 cc sesame oil twice a day during 20 weeks
The second intervention group will received 1 cc sweet almond oil ,twice a day during 20 weeks
The third intervention group will received 1 cc the combination of sweet almond oil and sesame oil ,twice a day during 20 weeks
The control group will received 1 cc placebo oil ,twice a day during 20 weeks.The placebo oil incudes distilled water and lubricant jel
Sponsors
Vice chancellor for research, Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1.Pregnant women with gestational age of 25-30 weeks aged 18 to 35 years old; pregnant women Age group between 18-35,2. Being nulliparous, 3.Having a single aliving fetous, 4. Gestational age 16-20 weeks (according last mensturation period or sonography ),5.Body mass index between 19.8-25, 6.Not having known coronic diseases such as adrenal disorders and diabetes (according woman telling ), 6. being literate, 7.Not using an other herbal or chemical drugs during pregnancy, 8. Not having any estriae on the abdomen ,arms,thighs and breasts 9.Being able to use the oils twice aday 10.Not going on any special diet. exclusion criteria :1.Having known skin diseases;2.polyhydraminious pregnancy;3.having allergy history to studied drugs;4.Having past surgical history on the abdomen;5.Having any malegnancy on the abdomen
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The incidence of estriae. Timepoint: At the end of the intervention. Method of measurement: The vising by educated midwives.;Severity of the estriae. Timepoint: At the end of the intervention. Method of measurement: Davey method.;The incidence of the irritation. Timepoint: At the end of the intervention. Method of measurement: Kamini method.;The severity of the irritation. Timepoint: At the end of the intervention. Method of measurement: Kamini method. | — |
Secondary
| Measure | Time frame |
|---|---|
| The comparision of the side events of the oils among intervention groups. Timepoint: At the end of the intervention. Method of measurement: The checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactKamrani Atefeh
Faculty of Nursing & Midwifery, Tabriz University of Medical Sciences
Outcome results
None listed