ArticlePlastic and reconstructive surgery. Global open2025
Tear Trough Rejuvenation With Injectable Biostimulatory Polynucleotides (VAMP).
Article in Plastic and reconstructive surgery. Global open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Comparative Effects of Injectable Biostimulatory Agents (Calcium Hydroxyapatite, New Cellular Treatment Factor, VAMP, and Human Exosomes) and Their Combination on Skin Regeneration.Aesthetic surgery journal. Open forum · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Tear trough rejuvenation presents a clinical challenge due to thin skin, superficial vasculature, and age-related volume loss. VAMP, manufactured by Prollenium, a polynucleotide-based biostimulatory injectable, is designed to support dermal regeneration and improve skin quality without volumizing excess. The objective of this study was to evaluate early clinical outcomes after VAMP injection in the tear trough area. Five healthy female patients (aged 35-50 y) of Middle Eastern and White descent were treated with 2 mL of VAMP (1 mL per side) using a 23G 30-mm SoftFil microcannula. The product was delivered via a combined microdroplet and linear threading technique to enhance distribution. Follow-up assessments were conducted at 1 week, 2 weeks, 1 month, and 3 months. Evaluation included standardized clinical photography, patient-reported satisfaction, and assessments of texture, tone, pigmentation, and contour. Mild to moderate improvements were observed in tear trough appearance, skin smoothness, and pigmentation. No adverse events were reported within the follow-up period. However, the limited sample size and short duration preclude definitive conclusions. Preliminary results suggested that VAMP may offer a promising option for tear trough rejuvenation. Further studies with larger cohorts and extended follow-up beyond 6 months are warranted.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.