Last reviewed · How we verify
NCT02992392
Comparison of the Clinical Effects of Two Tear Substitutes in Patients With Dry Eye Syndrome
NA trial testing Liposic in Dry Eye in 50 participants. Status unknown.
1 May 2017
Quick facts
| Lead sponsor | Sun Yat-sen University |
|---|---|
| Phase | NA |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 50 |
| Start date | 1 December 2016 |
| Primary completion | 1 May 2017 |
| Estimated completion | 1 June 2017 |
| Sites | 1 location across China |
Drugs / interventions tested
- Liposic — full drug profile →
- Tears Naturale Forte — full drug profile →
Conditions studied
- Dry Eye — all drugs for Dry Eye →
Sponsor
Sun Yat-sen University
Who can join
Adults 20 to 40, any sex, with Dry Eye. Healthy volunteers can join.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
scale of Schirmer I test
Time frame: up to 3 months after tear substitutes apply -
scale of corneal fluorescein staining
Time frame: up to 3 months after tear substitutes apply -
scale of noninvasive tear breakup time
Time frame: up to 3 months after tear substitutes apply -
scale of tear meniscus height
Time frame: up to 3 months after tear substitutes apply -
lipid layer grade
Time frame: up to 3 months after tear substitutes apply -
questionnaire of ocular surface disease index
Time frame: up to 3 months after tear substitutes apply
Sponsor's own description
With the potential to address evaporative dry eye, Liposic and Tears Naturale Forte have been developed in which phospholipid liposomes are delivered to the tear film via the surface of the closed eyelid. This study compare the effects of Liposic and Tears Naturale Forte application on the lipid and stability of the tear film in dry eye patients.
Publications & conference data
2 peer-reviewed publications reference this trial (live from Europe PMC):
-
Ocular Drug Delivery Barriers-Role of Nanocarriers in the Treatment of Anterior Segment Ocular Diseases.
Bachu RD, Chowdhury P, Al-Saedi ZHF, Karla PK, et al · · 2018 · cited 231× · PMID 29495528 · DOI 10.3390/pharmaceutics10010028 -
Recent advances and future challenges in nanosystems for ocular drug delivery.
Shahror RA, Fouda AY. · · 2025 · cited 1× · PMID 41478665 · DOI 10.1016/j.jpet.2025.103738
Verify or expand the search:
- PubMed search for NCT02992392
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Liposic
Trials testing the same drug.
- NCT03211351 — Effects of Two Tear Substitutes in Patients With Dry Eye Syndrome · NA · completed
Other recruiting trials for Dry Eye
Currently open trials in the same condition.
- NCT07366944 — PCOS and Problem of Eye Dryness: Is There a Benefit From Lifetyle Changes · NA · recruiting
- NCT07329712 — Comparing Tear Proteomics Profile in Dry Eye Disease pre-and Post-treatment With Low Level Light Therapy · recruiting
- NCT07266948 — Impact of TRYPTYR on a Patient's Quality of Life and Ability to Perform Work · Phase 4 · recruiting
- NCT07298811 — Preliminary Clinical Study of the Effectiveness and Safety of Ocular Surface Microbiota Transplantation in the Treatment · Phase 1, PHASE2 · recruiting
- NCT07135193 — Evaluation of the Protective Effects of Cordyceps Cicadae on Visual Function and Anti-Fatigue Performance in Esports Ath · NA · active not recruiting
Other Sun Yat-sen University trials
Trials by the same sponsor.
- NCT07255612 — Bone Marrow Protection, Safety, Efficacy of Trilaciclib and Eribulin in Locally Advanced or Metastatic TNBC(Triple-negat · Phase 2 · not yet recruiting
- NCT07371897 — Toripalimab ± Chemo as Neoadjuvant Therapy in LA-HNSCC: A Phase III Trial · Phase 3 · not yet recruiting
- NCT07489703 — SHR-A1811 + AK112 in HER2-Altered Advanced/Metastatic NSCLC · Phase 2 · not yet recruiting
- NCT07528209 — Neoadjuvant CAPOX With or Without Pucotenlimab Plus Selective Radiotherapy for Locally Advanced Rectal Cancer · Phase 3 · recruiting
- NCT07522281 — Evaluation of an Undisturbed Embryo Culture System for Embryo Development in IVF/ICSI Cycles · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02992392 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Sun Yat-sen University
- Last refreshed: 14 December 2016
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02992392.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing