Skip to content

Prevention and Treatment of Stretch Marks With Stratamark™

Assessment of Efficacy, Safety and Tolerability of Stratamark® (Innovative Self-drying Silicone Gel) in the Treatment and Prevention of Striae Distensae

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03377231
Enrollment
272
Registered
2017-12-19
Start date
2013-07-11
Completion date
2016-05-16
Last updated
2017-12-20

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

Conditions

Stretch Mark

Keywords

Pregnancy, Striae gravidarum, Striae distensae, Women's health

Brief summary

Stretch marks (striae distensae) are a form of scarring that is a natural result of pregnancy, obesity and in some instances occur due to puberty or steroid use. For some people, the stretch marks do not cause a problem, but in many circumstances they can cause physical symptoms such as itchiness, tenderness and pain. For many people stretch marks are also embarrassing and can have detrimental effects on a patient's mood and self-esteem. Stretch marks that result from pregnancy most commonly occur on the abdomen, breasts and thighs. Topical silicone gel was developed nearly thirty years ago to be used in the treatment of widespread hypertrophic scars (abnormal scars, which may be red or raised/depressed itchy or painful). Since this time it has been used successfully on most scar types. . Since stretch marks are a form of scarring it is thought that topical silicone gel may be helpful for this scar type also. Stratamark™ has been developed using different forms of silicone polymers, in a gel format, that dries to form a very thin and flexible silicone gel sheet making it a convenient therapy for the treatment and prevention of stretch marks. The aim of this clinical research study is to prove or disprove the efficacy, safety and tolerability of Stratamark™ in the prevention and treatment of stretch marks. In addition, the knowledge gained from this study may be of benefit to many future patients

Interventions

DEVICEStratamark®

Film-forming dressing for the prevention and treatment of stretch marks.

Sponsors

Stratpharma AG
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Intervention model description

The study involved the use of Stratamark® in prevention and treatment of stretch marks in 2 study arms.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Prevention arm - Inclusion Criteria: * Healthy pregnant woman (nulliparous or multiparous) entering into their third trimester (26-28 weeks, visit 1) * Not having striae on their abdomen at the time of trial enrollment Prevention arm -

Exclusion criteria

* Any significant medical or surgical conditions * Current medications liable to interfere with study results or change the skin's response to therapy Treatment arm - Inclusion Critera: • Confirmed SD on their abdomen post-delivery Treatment arm -

Design outcomes

Primary

MeasureTime frameDescription
Product efficacy in prevention of stretch marks5 monthsInvestigator-assessed prevalence of stretch marks in the patients treated with Stratamark vs. a literature-based control group. Measurement tool: dichotomous scale for the occurrence of stretch marks (0 no stretch marks - 1 appearance of stretch marks).
Product efficacy in treatment of stretch marks6 monthsInvestigator-assessed improvement in stretch marks severity of patients treated with Stratamark from baseline to last assessment. Measurement tool: likert scale for stretch marks severity (0 to 6 - 0 being no stretch marks and 6 being severe).

Secondary

MeasureTime frameDescription
Product efficacy in treatment of stretch marks6 monthsInvestigator-assessed improvement in stretch marks color of patients treated with Stratamark from baseline to last assessment. Measurement tool: likert scale for stretch marks color assessment (-4 to +4 - -4 being stark white compared to surrounding skin and +4 being purple). 0 being normal skin color, is considered to be the optimal value.
Severity of stretch marks developed in prevention5 monthsInvestigator-assessed severity of stretch marks developed in prevention patients. Measurement tool: likert scale for stretch marks severity (0 to 6 - 0 being no stretch marks and 6 being severe).
Patient evaluation of stretch marks in treatment6 monthsPatient-perceived change in color and noticeability of stretch marks at trial completion. Measurement tool: likert scale for stretch marks patient evaluation (-4 to +4 - -4 being much worse and +4 being cleared).
Patient product evaluation in treatment of stretch marks6 monthsPatient-perceived product efficacy, tolerability, ease of use and feeling on skin at trial completion. Measurement tool: likert scale for product evaluation (0 to 4 - 0 being unsatisfactory and 4 being excellent).
Patient product evaluation in prevention of stretch marks5 monthsPatient-perceived product efficacy, tolerability, ease of use and feel on skin at trial completion. Measurement tool: likert scale for product evaluation (0 to 4 - 0 being unsatisfactory and 4 being excellent).

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026