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CompletedNCT07919223ClinicalTrials.gov record

Vitamin B Complex as Adjunct Therapy for Moderate-to-Severe Dry Eye Disease

Dry Eye Disease · Dry Eye

THE QUICK READ

What this study involves

The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.

Study type
Interventional
Phase
Not applicable
Age range
18 years - 60 years
Sex eligible
All sexes
Healthy volunteers
Not accepted
Participants
56 Actual

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

This randomized controlled trial evaluated whether adding an oral vitamin B complex (thiamine, pyridoxine, and cyanocobalamin) to preservative-free artificial tears improves signs and symptoms of moderate-to-severe dry eye disease more than artificial tears alone. Adults aged 18-60 years with moderate-to-severe dry eye were randomly assigned to receive either artificial tears four times daily (control group) or the same artificial tears plus a once-daily vitamin B complex tablet for two months. The main outcomes measured were symptom scores (OSDI), tear meniscus height, tear break-up time, and Schirmer test results. The study was conducted at King Saud University in Riyadh, Saudi Arabia.

Read the full description

Dry eye disease is a common multifactorial condition of the ocular surface characterized by tear film instability, hyperosmolarity, and inflammation. B-complex vitamins (especially vitamins B1, B6, and B12) act as coenzymes in neuronal and cellular metabolism and may support ocular surface health and reduce neuropathic ocular pain.

This prospective, randomized controlled trial was conducted at the College of Applied Medical Sciences Clinics, King Saud University, between January and June 2023. Eligible participants were adults aged 18-60 years with moderate-to-severe dry eye disease (tear break-up time ≤ 10 seconds and Schirmer test \< 10 mm/5 min). Exclusion criteria included corneal disease, previous refractive surgery, contact lens wear, glaucoma, diabetic retinopathy, optic neuropathy, uveitis, current use of corticosteroids, immunomodulatory agents, antihistamines, or any ongoing dry eye treatment.

Participants were randomly assigned to one of two groups:

  • Group A (Control): Preservative-free artificial tears (Refresh Plus®, 0.5% carboxymethylcellulose) four times daily for two months.
  • Group B (Treatment): The same artificial tears plus one daily oral tablet of vitamin B complex (Neurorubine®: thiamine 200 mg, pyridoxine 50 mg, cyanocobalamin 1 mg) for two months.

Clinical assessments were performed at baseline and after two months. Outcome measures included:

  • Ocular Surface Disease Index (OSDI) score
  • Tear meniscus height (TMH)
  • Non-invasive keratograph tear break-up time (NIK-TBUT)
  • Fluorescein tear break-up time (fTBUT)
  • Schirmer test (without anesthesia)
  • Patient treatment satisfaction questionnaire

A total of 56 participants (28 per group) completed the study. Both groups showed significant improvement in OSDI scores. The combined therapy group demonstrated superior improvements in tear meniscus height and non-invasive tear break-up time compared with artificial tears alone.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

  • Adults aged 18 to 60 years
  • Male or female
  • Diagnosis of moderate-to-severe dry eye disease defined as:
  • Tear Break-Up Time (TBUT) ≤ 10 seconds
  • Schirmer test \< 10 mm/5 minutes
  • Willing and able to provide written informed consent
  • Willing to comply with study procedures and follow-up visits

Exclusion Criteria:

Presence of corneal disease

  • History of refractive surgery
  • Current contact lens wear
  • Glaucoma
  • Diabetic retinopathy
  • Optic neuropathy
  • Uveitis
  • Current chemotherapy or radiotherapy
  • Current use of systemic corticosteroids or immunomodulatory agents
  • Current use of antihistamines
  • Any ongoing treatment for dry eye disease
  • Any other condition that, in the opinion of the investigator, would make the participant unsuitable for the study
Understand screening

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment
Random assignment
Masking
No masking
Artificial Tears Alone (Control)

Participants received preservative-free artificial tears (Refresh Plus®, 0.5% carboxymethylcellulose) four times daily for two months.

Drug: Carboxymethylcellulose Sodium 0.5% Eye Drops

Artificial Tears + Vitamin B Complex

Participants received preservative-free artificial tears (Refresh Plus®, 0.5% carboxymethylcellulose) four times daily plus one daily oral tablet of vitamin B complex (Neurorubine®) for two months.

Drug: Carboxymethylcellulose Sodium 0.5% Eye Drops · Dietary Supplement: Vitamin B Complex

Carboxymethylcellulose Sodium 0.5% Eye Drops DRUG

Preservative-free artificial tears, one drop in each eye four times daily for two months.

Vitamin B Complex DIETARY_SUPPLEMENT

Oral tablet containing thiamine 200 mg, pyridoxine 50 mg, and cyanocobalamin 1 mg, taken once daily for two months.

Prepare your questions

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Change in Ocular Surface Disease Index (OSDI) Score

Time frame: Baseline and 2 months

The Ocular Surface Disease Index (OSDI) is a validated 12-item questionnaire used to assess dry eye symptoms and their impact on vision-related functioning. The total score ranges from 0 to 100, with 0 representing no symptoms and 100 representing the most severe symptoms. Higher scores indicate greater dry eye disease severity and worse outcomes.

The conventional OSDI severity categories are:

  • 0-12: Normal
  • 13-22: Mild
  • 23-32: Moderate
  • 33-100: Severe

Secondary measures

Change in Tear Meniscus Height (TMH)

Time frame: Baseline and 2 months

Change in Tear Meniscus Height (TMH), measured in millimeters (mm), from baseline to the specified follow-up assessment. TMH is an objective indicator of tear volume. Higher TMH values generally indicate greater tear volume and are considered a favorable outcome in patients with aqueous-deficient dry eye disease. The measurement is recorded as a continuous variable. No fixed minimum or maximum values are specified for this outcome measure.

Higher values Generally indicate greater tear volume and a better outcome Outcome calculation Follow-up TMH minus baseline TMH

Change in Non-Invasive Keratograph Tear Break-Up Time (NIK-TBUT)

Time frame: Baseline and 2 months

Non-Invasive Keratograph Tear Break-Up Time (NIK-TBUT), measured in seconds (s), from baseline to the specified follow-up assessment. NIK-TBUT is an objective measure of tear film stability, determined using a non-invasive keratograph. The measurement is recorded as a continuous variable. Higher values indicate longer tear film stability and generally represent a better clinical outcome. No fixed minimum or maximum values are specified for this measurement.

Change in Fluorescein Tear Break-Up Time (fTBUT)

Time frame: Baseline and 2 months

Fluorescein Tear Break-Up Time (fTBUT), measured in seconds (s), from baseline to the specified follow-up assessment. fTBUT is an objective clinical measure of tear film stability, determined by measuring the time elapsed between fluorescein instillation and the appearance of the first break in the tear film. The measurement is recorded as a continuous variable. Higher values indicate greater tear film stability and generally represent a better clinical outcome. No fixed minimum or maximum values are specified for this measurement.

Change in Schirmer Test Score

Time frame: Baseline and 2 months

Schirmer Test, measured in millimeters (mm) of wetting of the standardized filter paper strip over 5 minutes, from baseline to the specified follow-up assessment. The Schirmer test is an objective measure of aqueous tear production. The measurement is recorded as a continuous variable, with values typically ranging from 0 to 35 mm over 5 minutes, depending on the test strip and measurement protocol. Higher values indicate greater tear production and generally represent a better clinical outcome in patients with aqueous-deficient dry eye disease.

Patient Treatment Satisfaction

Time frame: 2 months

Patient Treatment Satisfaction was assessed using a patient-reported satisfaction scale at the specified follow-up assessment. The score reflects the participant's overall satisfaction with the assigned treatment. Higher scores indicate greater treatment satisfaction and a more favorable patient-reported outcome. The minimum and maximum possible scores depend on the scale used.

No results are flagged as posted.

Review the complete result tables and limitations in the official record.

Open official results ↗

Research locations (1)

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1 locations

College of Applied Medical Sciences Clinics, King Saud UniversityRiyadh, Saudi ArabiaStatus unknown

Study team and timeline

Lead sponsor
Rania Fahmy
Study start
Jan 1, 2023 Actual
Primary completion
Jun 30, 2023 Actual
Study completion
Jun 30, 2023 Actual
First posted
Nov 5, 2026 Actual
Last updated
Nov 10, 2026 Actual

Official study contacts

No central contact is listed. Check the locations and the official record.

Official study title

Vitamin B Complex as a Therapeutic Adjunct for Moderate-to-Severe Dry Eye Disease in Otherwise Healthy Subjects: A Randomized Controlled Trial

A HUMAN NEXT STEP

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Source: ClinicalTrials.gov API v2. Information is submitted by sponsors and investigators. NLM does not approve the safety or science of all listed studies. Registry disclaimer.

Retrieved: Nov 11, 2026 · Last registry update: Nov 10, 2026