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Ayurveda-Based Integrative Management Of Diabetic Retinopathy

Clinical Evaluation Of Ayurveda- Based Integrative Management Of Diabetic Retinopathy - DRAIM

Status
Recruiting
Phases
Phase 3Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2018/09/015683
Enrollment
40
Registered
2018-09-11
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: H350- Background retinopathy and retinalvascular changes Health Condition 2: H352- Other non-diabetic proliferative retinopathy

Interventions

Intervention1: Nishoshiradi taila, Anutaila or Ksheerabala101 oil, Lodhravasadi Grutha, Nishakatakadi Kashayam, Kaalashakadi Kashayam, Vasaguduchyadi Kashayam.: -Shiroabhyanga (Head massage) for 20min

Sponsors

Dr GG Gangadharan
Lead Sponsor
Dr Sribhargava Natesh
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: -Non insulin dependent diabetes mellitus -Mild to Moderate Diabetic Retinopathy

Exclusion criteria

Exclusion criteria: -Patients with H/O Previous treatment for diabetic retinopathy, including laser and Anti- VEGF drug. -Presence of severe non-proliferative diabetic retinopathy or proliferative diabetic retinopathy -Other ophthalmic conditions such as Cataract etc. -Presence of diabetic nephropathy or cardiovascular disease -Pregnancy or Lactation -HbA1C >10% -Statin Use

Design outcomes

Primary

MeasureTime frame
Significant decrease in the frequency and severity of manifestations of diabetic retinopathy(DR), including cotton wool spots, dot and blot hemorrhages and macular exudatesTimepoint: Assessment done at baseline and 6months with Optical Coherence Tomography(OCT) Fundus Photography(FP), Visual Acuity(V/A) and Visual Function Questionnaire(VFQ) will be done at baseline, three and six months.

Secondary

MeasureTime frame
-Significant reduction of macular thickness measured using OCT in patients with diabetic macular edema. -No significant loss of vision,i.e reduction of visual acuity by 2 lines or more on the LogMAR chart, not attributable to other visual disorders such as cataract. -Improvement or no worsening of visual function and quality of life at the end of the Study period.Timepoint: Assessment done at baseline and 6months with Optical Coherence Tomography(OCT) Fundus Photography(FP), Visual Acuity(V/A) and Visual Function Questionnaire(VFQ) will be done at baseline, three and six months.

Countries

India

Contacts

Public ContactDr GG Gangadharan

Ramaiah Indic Specialty Ayurveda Restoration Hospital

msricaimresearch@gmail.com9448278900

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026