RecruitingNCT07467837
Prevention of Stretch Marks in Expectant Mothers
Prevention (Reduction of Incidence) of Stretch Marks in Expectant Mothers
Sponsor
Stratpharma AG
Enrollment
10,000 participants
Start Date
Feb 24, 2026
Study Type
OBSERVATIONAL
Conditions
Summary
PRIME Mothers is a national observational trial designed to evaluate patient outcomes with Stratamark® for the prevention of stretch marks during pregnancy and the postpartum period. The study is designed to fit seamlessly into routine clinical practice, with digital follow-up and home resupply, minimising clinic involvement.
Eligibility
Sex: FEMALEMin Age: 18 Years
Inclusion Criteria6
- Pregnant women at any gestational age.
- Participants who are in good health, including those that are carrying multiples, who are 18 years of age or older.
- Confirmed absence of pre-existing stretch marks on the abdomen.
- Agree to apply Stratamark according to the prescribed protocol for the duration of the study.
- Ability to complete remote online surveys via an electronic device.
- Provide signed informed consent to participate in the study.
Exclusion Criteria6
- Visible stretch marks on the abdomen prior to enrollment.
- Pre-existing skin conditions (e.g., eczema, psoriasis), on the abdomen that could interfere with product application or assessment of stretch marks.
- Known hypersensitivity or allergy to any of the ingredients in Stratamark.
- Use of other topical treatments on the abdomen, including but not limited to oils, or creams targeting stretch mark prevention.
- Participants unable to give informed consent, or unable to have written consent provided on their behalf.
- Participants who cannot administer the treatment or have the treatments administered as per the directions for use.
Interested in this trial?
Get notified about updates and connect with the research team.
Interventions
DEVICEStratamark
Topical film-forming silicone gel
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07467837
Related Trials
Outpatient Induction of Labour Using a Double Balloon Transcervical Catheter in Low-risk Pregnant Women: a Two-centre Open Prospective Randomised Controlled Trial - OutCRIB
NCT072655182 locations
Prenatal Treatment of Congenital Cytomegalovirus Infection With Letermovir Versus Valaciclovir
NCT054465711 location
Effect of Helfer Skin Tap and Cold Application on Pain and Hemodynamics During Vaccination
NCT069766321 location
Ultra-early Identification of Fetal Chromosomal Characteristics From Extravillous-trophoblast Cells
NCT065235431 location
Evaluation of the Absence of Intraoperative Bladder Catheterization in Case of Planned Cesarean Section
NCT063575462 locations