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Valuating the Effects of Oligopin Supplementation on the Turnover of Bone Formation and Antioxidant Changes in Postmenopausal Osteopenic Women: A Randomized Double-blind Clinical Trial With Placebo-concurrent Controls
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 18, 2026
NCT ID
NCT03260803
Status
COMPLETED
Phase
Phase 3
Sponsor
Tehran University of Medical Sciences
Executive brief
Investment-Ready Snapshot
The clinical trial sponsored by Tehran University of Medical Sciences investigates the efficacy of oligopin, a pine bark extract rich in polyphenols, in improving bone turnover and reducing oxidative stress in postmenopausal women with osteopenia. Given the high prevalence of osteopenia and osteoporosis in Iran, this study addresses a significant unmet medical need. If successful, oligopin could position itself as a natural alternative or adjunct to existing osteoporosis therapies, potentially capturing market share in the growing segment of herbal and phytochemical-based treatments. The results may also attract interest from pharmaceutical companies looking to expand their portfolios in bone health and women's health sectors. However, the competitive landscape includes established osteoporosis treatments, necessitating a clear differentiation strategy for oligopin.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03260803
Indication
Osteopenia
Modality
small molecule
Target
Bone turnover markers, oxidative stress modulation via antioxidant pathways (MnSOD, catalase, Nrf2 expression).
Intervention
Oligopin, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.