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Development and validation of a clinician-reported abdominal stretch mark scale

Development and validation of a clinician-reported abdominal stretch mark scale

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121973
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-04-07
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Abdominal stretch marks

Interventions

Abdominal stretch mark observation group:None

Sponsors

Chinese Academy of Medical Sciences, Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Age range: 18 - 50 years (inclusive), diagnosed with abdominal stretch marks by clinical assessment; 2. More than 6 months postpartum (ensuring that the stretch mark condition has stabilized); 3. Skin Fitzpatrick classification: Type II - IV; 4. Voluntary participation in this clinical study and signing the informed consent form for participants.

Exclusion criteria

Exclusion criteria: 1. The assessment area contains tattoos, scars, skin lesions, or other streaks caused by non-pregnancy-related factors as determined by the researchers and which may affect the judgment; 2. The assessment area has received previous treatment, such as injections for filling or abdominal liposuction within the past two years; 3. Within the past six months, the assessment area has undergone laser, micro-needle, or retinoic acid drug treatments; 4. Currently taking or planning to take medications that may affect the skin condition, such as systemic use of hormones, etc.; 5. Has a previous history of mental illness and has been assessed by the researchers as not suitable for inclusion; 6. Within the 5 half-lives after the previous clinical research involving intervention devices or the last medication use in a drug clinical study, participated in another intervention device clinical research or drug clinical study; 7. The researcher deems it inappropriate to participate in this clinical study.

Design outcomes

Primary

MeasureTime frame
Abdominal stretch marks morphology;Abdominal stretch mark pigment;Texture of abdominal stretch marks;Distribution of abdominal stretch marks;

Countries

China

Contacts

Public ContactXiao Long

Chinese Academy of Medical Sciences, Peking Union Medical College Hospital

pumclongxiao@126.com+86 13810193175

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026