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Safed Daag

Randomized Controlled Clinical Study to Evaluate Efficacy of Siddhartak Udvartan with Bakuchi Ghan in Shvitra - Nil

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/01/079807
Enrollment
156
Registered
2025-01-30
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: L80- Vitiligo

Interventions

None listed

Sponsors

Mohd Khalid Abdul Aziz Ambekar
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients fulfilling the criteria of diagnosis of Shvitra irrespective of sex,religion and economic status. 2.Newly developed patches or macules(within one year). 3.Patients of Shvitra having VASI Score less than 50%.

Exclusion criteria

Exclusion criteria: 1.Psychotic patients. 2.Whole body affected with Shvitra. 3.Shvitra on lips,on palms of hand,sole of feet and white haired patches. 4.Secondary to burn. 5.On private parts. 6.Pregnancy and lactating mother. 7.Patients having hereditary Shvitra. 8.Post injury Shvitra 9.Patient receiving Allopathic or other treatment for Shvitra. 10.Patient having hypersensitive skin to any external application.

Design outcomes

Primary

MeasureTime frame
Shwet Mandal 1) Colour of lesion- Grade- 0-Normal 1-Black 2-Red 3-Pink 4-White 2) Shape of lesion- Grade- 0-Totally cured 1-Reduced to some extend 2-No change in shape Timepoint: follow up of all patients will be taken after every 15 days for three months

Secondary

MeasureTime frame
Subjective Criteria 1)Kandu(Itching)- Grade- 0- No Itching 1- Itching less than 1 hour(Mild) 2- Itching 1-2 hrs(Moderate) 3- Itching more than 2 hrs(severe) 2)Rukshata(Dryness)- 0- No dryness 1- Only roughness of skin with no fissure, no scaling and no pain 2- Roughness with scaling.No fissure,no pain 3- Roughness, scaling and. fissure with or without pain Timepoint: All subjective criterias will be assisted every 15 days for 3 months;3) Daha- Grade- 0-No daha 1-Occaisional burning sensation at lesion site,not felt during daily physical activities and during sleep 2-Continues and bearable daha but not felt during daily physical activities and sleep 3-Continues and unbearable daha,felt during daily physical activities,sleep may or may not disturbedTimepoint: All subjective criterias will be assisted every 15 days for 3 months;Objective Criteria 1) Lesion margin colour- Grade- 0-Normal 1-Black 2-Red 3-Pink 4-White 2) Colour of overlying hairs- Grade- 0- Normal 1-Abnormal(Change in colour) 3) Location of lesion- Grade- 0-No lesion 1-Single location 2-2-4 location 3-More than 4 locationsTimepoint: All objective criterias will be assisted every 15 days for 3 months;Investigations HaemogramTimepoint: Haemogram will be done before and after study(i.e before and after three months)

Countries

India

Contacts

Public ContactMohd Khalid Abdul Aziz Ambekar

CSMSS Ayurved College

dr.shrikantgdeshmukh@gmail.com9921553999

Outcome results

None listed

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