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Efficacy of platelet rich plasma in dry eye patients who had not responded to autologous serum treatment

Efficacy of platelet rich plasma in dry eye patients who had not responded to autologous serum treatment

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201020002
Enrollment
25
Registered
2020-10-20
Start date
2020-10-18
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Dry eye disease Dry eye disease Platelet rich plasma Ocular surface disease

Interventions

Platelet rich plasma of participants will be used 6 times/day for 3 months
Experimental Biological/Vaccine

Sponsors

Ratchadaphaiseksomphot fund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Aged 18&#45;80 years OSDI scores at least 13 with corneal staining > 5 spots or tear break&#45;up time < or = 5 seconds in patients treated with autologous serum at least 3 months

Exclusion criteria

Exclusion criteria: Lid problems including lagophthalmos&#44; ectropion&#44; entropion trichiasis&#44; distichiasis&#44; epiblepharon Previuos history of ocular infection in 3 months Possibility to have problem with follow&#45;up Possibility to have problem with applying platelet rich plasm Herpetic keratitis Thrombocytopenia&#44; sepsis&#44; chronic liver disease&#44; anti&#45;coagulation therapy including warfarin&#44; dabigatran&#44; heparin Hb < 11 mg/dl or Hct < 33% or platelet < 140&#44;000 cell/mm2 History of ocular surgery within 1 month

Design outcomes

Primary

MeasureTime frame
Dry eye symptoms 1&#44; 2&#44; 3 months Ocular surface disease index score

Secondary

MeasureTime frame
Corneal staining 1&#44; 2&#44; 3 months Cornea NEI scale,Conjunctival staining 1&#44; 2&#44; 3 months Conjunctival NEI scale,Tear break up time 1&#44; 2&#44; 3 months Tear break up time,Tear production 1&#44; 2&#44; 3 months Schirmer test,Subbasal and dendritic cell density 1&#44; 2&#44; 3 months In vivo confocal microscopy,Side effect 1 wk&#44; 1&#44; 2&#44; 3 months description

Countries

Thailand

Contacts

Public ContactVannarut Satitpitakul

Faculty of Medicine&#44; Chulalongkorn University

vannarut.s@chula.ac.th+6622564142

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026