Striae gravidarum Skin and Connective Tissue Diseases
Conditions
Interventions
Control group: left abdomen of each participant, no treatment.
Intervention group: right abdomen of each participant, PRP stem cell transplantation.
Transplantation: 1
Sponsors
Shenyang Maternal and Child Care Service Center
Shenyang Engineering Technology R&D Center of Cell Therapy Co., Ltd
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: 1. Pregnant women with striae gravidarum 2. Full-term or cesarean delivery 3. Aged 23 to 30 years
Exclusion criteria
Exclusion criteria: 1. Participant in other ongoing clinical trials 2. Tested positive for hepatitis B, hepatitis C, HIV, syphilis, EBV, or CMV 3. History of severe allergic reactions or adverse reactions to medication
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual changes measured using abdomen photos at baseline, the 7th day after each transplantation (i.e., day 8, 17, and 27 post-delivery), month 2, and month 3 post-delivery | — |
Secondary
| Measure | Time frame |
|---|---|
| Measured at baseline, day 8, 17, 27, month 2, and month 3 post-delivery: 1. Pain caused by striae gravidarum measured using self-reporting questionnaires 2. Pruritus caused by striae gravidarum measured using self-reporting questionnaires | — |
Countries
China
Contacts
Public ContactYutong Ge
Outcome results
None listed