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Clinical Trials/CTRI/2023/05/052349
CTRI/2023/05/052349
Active, not recruiting
Phase 2

A Clinical study to evaluate the efficacy of Khasa beeja tailam (Seed oil of Papaver somniferum) in Darunaka Vyadhi. - A Clinical study to evaluate the efficacy of khasa beeja tailam (Seed oil of Papaver somniferum) in Darunaka Vyadhi

Central council for Research in Ayurveda Sciences0 sites0 target enrollmentTBD
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Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Central council for Research in Ayurveda Sciences
Status
Active, not recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Central council for Research in Ayurveda Sciences

Eligibility Criteria

Inclusion Criteria

  • •1\. Subjects in General good health of either sex. (Subjects without other specific health
  • •complaints.)
  • •2\. Subjects within the age group of 18\-55 years.
  • •3\. Subjects willing to give a written informed consent and willing to abide by and
  • •comply with the study protocol.
  • •4\. Subject exhibiting a slight to moderate dandruff or Seborrheic dermatitis of scalp on
  • •the total adherent and non adherent score after clinical examination, on Day 0\.
  • •5\. Subject having stopped any possible antidandruff treatment at least 2 weeks prior to

Exclusion Criteria

  • •1\. Associated with other dermatological conditions such as psoriasis etc.
  • •Other Systemic illness.
  • •2\. Pregnant, lactating mothers, menopausal women.
  • •3\. Any Immuno\-compromised patients and uncontrolled Diabetes
  • •4\. Systemic treatment with corticosteroids, antibiotics, immune\-suppressants etc, or any
  • •modern treatment within 3 months before of this trial.
  • •5\. Subjects who have undergone hair growth treatment within 3 months before screening
  • •into the study. Subjects, who have history of alcoholism, smoking, crash dieting and/or
  • •psychiatric disorder including trichotillomania. Subjects who have had hair
  • •transplantation, who have taken pharmaceutical product which cause hirsutism(ex.phenytoin) and finasteride for androgenic alopecia, under medical treatment for

Outcomes

Primary Outcomes

Not specified

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