Ganyan-1 in Dry Eye

ConditionsDry EyeTCM
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorBeijing Tongren Hospital

About this trial

Ganyan -1 for the patients with dry eye

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

History systemic autoimmune diseases and ocular/periocular malignancy.

Clinically relevant slitlamp findings or abnormal lid anatomy.

Active ocular allergies and active infection.

Pregnant or lactating women.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Ganyan1

    Drug

    During the treatment period, participants will receive the following Chinese herbal granules, including Chrysanthemum, Dendrobium, Salvia miltiorrhiza, Gypsum Fibrosum, and Goji berries, administered twice daily at a dose of 10 g per time for a duration of 4 weeks.

  • Sodium Hyaluronate

    Drug

    Participants received 0.1% sodium hyaluronate eye drop

  • 1/2Ganyan1

    Drug

    During the treatment period, participants will receive the following Chinese herbal granules, including Chrysanthemum, Dendrobium, Salvia miltiorrhiza, Gypsum Fibrosum, and Goji berries, administered twice daily at a dose of 5 g per time for a duration of 4 weeks.

  • Placebo

    Drug

    Participants will receive the following placebo Chinese herbal granules, administered twice daily at a dose of 10 g per time for a duration of 4 weeks.

Treatment groups

219 Participants
are divided into 3 treatment groups
Group A: Ganyan1Experimental treatment 2 interventions
Group B: 1/2Ganyan1Experimental treatment 2 interventions
Group C: PlaceboPlacebo comparator 2 interventions

Trial outcomes

Primary outcomes

1

OSDI

The Ocular Surface Disease Index (OSDI) includes 12 questions grouped by poor symptoms and visual disturbance (light sensitivity, eyes feel gritty, painful or sore eyes, blurred vision or poor vision); visual function/tasks (problems when reading, driving at night, working on a computer or watching TV); and environmental questions (problems in windy conditions, places/ areas with low humidity or areas that are air conditioned). The scores range from 0 to 100. On the basis of the score, the patient's symptoms can be categorized as normal (0-12), mild dry eye (13-22), moderate dry eye (23-32), or severe dry eve (33-100).

Time frame
Baseline, week 2, 4, 8, 12 and 16

Secondary outcomes

1

TBUT

Tear breakup time (TBUT) is a clinical test used to assess for evaporative dry eye disease. To measure TBUT, fluorescein is instilled into the patient's tear film and the patient is asked not to blink while the tear film is observed under a broad beam of cobalt blue illumination. The TBUT is recorded as the number of seconds that elapse between the last blink and the appearance of the first dry spot in the tear film, as seen in this progression of these slit lamps' photos over time. A TBUT under 10 seconds is considered abnormal.

Time frame
Baseline, week 2, 4, 8, 12 and 16
2

Schirmer

The Schirmer test is objectively used to measure tear secretion without anesthetized. A healthy eye should wet more than 10 mm of the standard filter strip in 5 minutes. The travel rate along the test strip is proportional to the tear production rate.

Time frame
Baseline, week 2, 4, 8, 12 and 16
3

SF-36

36-Item Short Form Health Survey (SF36) measures quality of life on the basis of eight dimensions or concepts that are frequently used in health studies. These eight dimensions are estimated from eight subscales that examine physical functioning (SF36-PF), role functioning-physical (SF36-RP), bodily pain (SF36-BP), general health (SF36- GH), vitality (SF36-VT), social functioning (SF36-SF), role functioning-emotional (SF36-RE), mental health (SF36-MH) and reported health transition (SF36-HT). Item responses were ranaina from 0 (best) to 100 (worst), with hiaher scores are equivalent to areater severity of better quality of life.

Time frame
Baseline, week 2, 4, 8, 12 and 16
4

SAS

The SAS is a 20-item self-report instrument designed to assess anxiety symptoms in clinical and research settings. This scale ranges from 20 to 80, with lower scores indicating better self-reported mental health and fewer anxiety symptoms.

Time frame
Baseline, week 2, 4, 8, 12 and 16

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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