Actively Recruiting

Age: 18Years +
FEMALE
NCT07467837

Prevention of Stretch Marks in Expectant Mothers

Led by Stratpharma AG · Updated on 2026-03-12

10000

Participants Needed

1

Research Sites

48 weeks

Total Duration

On this page

Sponsors

S

Stratpharma AG

Lead Sponsor

S

St Andrew's War Memorial Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Prevention of Stretch Marks in Expectant Mothers

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women at any gestational age
  • Good health, including those carrying multiples, aged 18 years or older
  • No pre-existing stretch marks on the abdomen
  • Agree to apply Stratamark as prescribed throughout the study
  • Able to complete remote online surveys using an electronic device
  • Provide signed informed consent to participate
Not Eligible

You will not qualify if you...

  • Visible stretch marks on the abdomen before enrollment
  • Existing skin conditions on the abdomen (e.g., eczema, psoriasis) that could affect treatment or assessment
  • Known allergy or hypersensitivity to any ingredient in Stratamark
  • Use of other topical treatments on the abdomen targeting stretch mark prevention
  • Unable to give informed consent or have consent provided on their behalf
  • Unable to apply or receive the treatment as directed

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Pelvic Medicine Centre, St Andrew's War Memorial Hospital

Brisbane, Australia

Actively Recruiting

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Research Team

A

Alexandra Zurlinden

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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