Evidence map›Paper›PMID 41613775›Full record

ArticleFrontiers in pharmacology2026

A comprehensive analysis of dry eye disease clinical trials (2000-2024): research trends and gaps.

Xiaohui Jiang, Boyue Xu, Ruxin Xu, Nanxin Wu, Shudong Tian, Haotian Peng, Yun-E Zhao

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Xiaohui Jiang *Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Boyue Xu *Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Ruxin XuEye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Nanxin WuEye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Shudong TianEye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Haotian PengEye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.
Yun-E ZhaoEye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University, Wenzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Dry eye disease (DED), also known as keratoconjunctivitis sicca (KCS), imposes a substantial global burden, yet the clinical trial landscape guiding therapeutic development remains incompletely characterized. Methods: We conducted a cross-sectional study mapping interventional dry eye disease trials (2000-2024) indexed in Trialtrove. We analyzed 1,171 prospectively registered trials with dry eye disease as the primary indication, characterizing design, phase, geography, sponsorship, endpoints, and therapeutics. Results: Trial activity rose steadily, peaking in 2023-2024, and was concentrated in the United States (n=773), followed by India (n=111), China (n=71), and Japan (n=58). Sponsorship was balanced between industry (45.5%) and academia (44.4%). Most trials were completed and in later phases (Phase 4: 40.3%; Phase 2: 25.0%; Phase 3: 17.0%). Adult cohorts predominated, yet 59.9% did not report severity strata, and where strata were prespecified, thresholds based on symptom questionnaires were heterogeneous. Monotherapy designs were most common (71.6%), with head-to-head comparisons in 22.4%. Frequently studied interventions included other ocular medications, ocular anti-inflammatory agents, and artificial tears. Primary endpoints centered on ocular surface staining, with the Ocular Surface Disease Index, tear film break-up time, and Schirmer's test commonly used. Discussion: These commonly used endpoints vary in psychometric validity and standardization, which can undermine data quality, complicate analysis and interpretation of individual trial results, and limit cross-trial comparability. Overall, the ecosystem appears mature but conservative, emphasizing later-phase, single-agent studies, traditional endpoints, and limited severity stratification and geographic diversity. Future trials should prespecify severity and subtype strata, use validated mechanism-aligned endpoints with standardized assessment windows and longer follow-up, and broaden geographic representation to improve generalizability and cross-trial comparability.

Indexed as

clinical trialsdry eye diseasegeographical distributionresearch trendstrial design

Identifiers

PMID41613775
PMCPMC12847023

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.