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A Prospective study to evaluate Effectiveness and safety of Microneedling Fractional Radiofrequency (MnRF) and Microneedling Fractional Radiofrequency (MnRF) with platelet rich plasma therapy(PRP) in the Treatment of Striae Distensae

Effectiveness and safety of Microneeding Fractional Radiofrequency (MnRF) and Microneedling Fractional Radiofrequency (MnRF) with platelet rich plasma therapy (PRP) in the Treatment of Striae Distensae-A randomized controlled trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071283
Enrollment
64
Registered
2024-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: L906- Striae atrophicae

Interventions

Intervention1: Microneedling Fractional Radiofrequency (MnRF): Group A – MnRF is given, one sitting,once in 4 weeks that is for 4 sittings - Week 0,4,8,12.Follow up pictures will be taken at week 16 a

Sponsors

SRM Medical College Hospital and research centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All Patients above 18 years of age attending SRM MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE Dermatology OPD, diagnosed with striae distensae. 2. Patients willing to refrain from all other oral and topical medications for striae distensae. 3. Patients providing voluntary informed and written consent for the explained treatment modality to be performed

Exclusion criteria

Exclusion criteria: 1. Patients who have received treatment for SD in the past 3 months. 2. Pregnant and lactating women. 3. Patients with active infections at the site. 4. Patients with history of photosensitive disorders like lupus erythematosus, dermatomyositis. 5. Patients with history of propensity for keloid formation and vitiligo.

Design outcomes

Primary

MeasureTime frame
Clinical assessment of improvement of striae according to Global Aesthetic Improvement Scale (GAIS), SDA scoring scale by a side by side comparison of Pre-operative and post-operative photographs taken at every visit and at the end of 4 weeks and 12weeks after the last session. Timepoint: Week 0, 4, 8, 12, 16, 24

Secondary

MeasureTime frame
Patient satisfaction score at the end of the studyTimepoint: 24th week

Countries

India

Contacts

Public ContactVarshini N R

SRM Medical College Hospital and Research Centre

leecutis@gmail.com9840168711

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026