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CompletedNCT01321645Updated Oct 23, 2012

Efficacy of Azadirachta Indica (Homoeopathic Medicine) in Treatment of Acne Vulgaris

A Phase 1 interventional study of Azadirachta Indica in Acne Vulgaris, sponsored by Miglani, Anjali. Completed at 1 site in India. Open to participants aged 12 Years to 25 Years. Per ClinicalTrials.gov, last updated 2012-10-23.

Sponsored by Miglani, Anjali · Phase 1, Interventional, and Treatment

Phase
Phase 1
Study type
Interventional
Enrollment
31
Allocation
Not applicable
Ages
12 Years to 25 Years
Sex
All
01

Study summary

Acne is one of the most common skin problems in teenagers and adolescents. There are many lesser known homoeopathic medicines which have been mentioned in the literature for treatment of acne but their potential has not been properly assessed /documented and therefore these medicines don't form a part of many prescriptions. As a part of this study,efficacy of Azadirachta Indica will be studied in the treatment of Acne vulgaris

02

Conditions studied

  • Acne Vulgaris

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Keywords

  • Acne Vulgaris
  • Homoeopathy
  • Homeopathy
  • Azadirachta Indica
03

In context

Acne Vulgaris

730 studies on the registry are indexed under Acne Vulgaris; 86 are open to participants now.

This study's enrollment of 31 is below the median of 69 across 628 interventional studies indexed under Acne Vulgaris.

Browse Acne Vulgaris studies →

Lead sponsor

Miglani, Anjali is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
12 Years to 25 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Males and females between 12 to 25 years of age
  • Presence of inflammatory and non-inflammatory lesions
  • Able to follow-up according to protocol
  • Patients not taking any medication for treatment of Acne in preceding one month.

Exclusion criteria

Exclusion Criteria:

  • Acne Conglobata
  • Pregnant or Breast feeding females or females having intention of becoming pregnant
  • Significant systemic disease
  • Any drug/ alcohol addiction
  • History of chronic diseases treated with medications in the preceding month which might affect acne condition and treatment outcome
05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
31 participants (actual)

Interventions

  • DrugAzadirachta Indica

    To start with subjects will be prescribed Azadirachta Indica in 6 potency to be taken in form of pills 4 times a day for seven days. Dosage and frequency will be changed, if required, based on the condition of subject and their response according to homoeopathic principles.

06

What researchers measure

Primary outcomes

  1. percent change in acne lesion counts from the Baseline

    Time frame: 6 months

Secondary outcomes

  1. change in quality of life of subjects from baseline

    Change in Quality of life will be assessed based on Quality of Life Questionnaire to be filled by subjects at the start of Treatment and at the end of time frame.

    Time frame: 6 months

07

Study locations

1 site
  • Delhi Government Health Centre - Homoeopathic Dispensary - Sector 12, Dwarka
    New Delhi, Delhi 110075, India
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 23, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01321645
Lead sponsor
Miglani, Anjali
Collaborators
Department of Indian Systems of Medicine and Homeopathy
Responsible party
Dr. Anjali Miglani (Senior Medical Officer, Miglani, Anjali) — Principal investigator
First posted
Mar 23, 2011
Start date
Mar 2011
Primary completion
May 2012
Completion
Jun 2012
Last update
Oct 23, 2012

Study contacts

Anjali Miglani, BHMS
principal investigator · Department of Indian Systems of Medicine and Homeopathy

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2012. You cannot join it, but the record below documents what was studied.

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