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Clinical Trials/CTRI/2025/01/079808
CTRI/2025/01/079808Not yet recruitingNot Applicable

Pharmaceutico-Analytical study and clinical evaluation of modified cream form of Sahachara Ghrita on Mukhdushika with special reference to Acne vulgaris:A Randomized Controlled Trial

Dr Manjusha Suresh Uikey1 site in 1 country60 target enrollmentStarted: February 15, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
Prepare Sahachara Ghrita and its cream form, to study its organoleptic, physio-chemical, phyto-chemical parameters and clinically compare its effect with Shalmali Kantaka Lepa on Mukhadushika.

Study Overview

Brief Summary

In the present study, total 60 participants will be taken for trial dividing them in 2 equal groups.

Grp-A will receive the trial drug Modified cream form of Sahachara Ghrita and Grp-B will receive the controlled drug Shalmali Kantaka Lepa

for external application for 30 days.

Follow up will be taken on Day-0th,15th,30th,45th.

Result will be concluded based on assessment criteria.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 30.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patient having symptom of Mukhadushika.
  • Shalmali Kantak like eruptions 2)Saruja pidika(painful acne) 3)Ghana Pidikas (hard and thick acne) 4)Medogarbha Pidikas (acne filled with oil/sebum/pus) 5)Shotha (Inflammation) 6) Patient having symptom of acne vulgaris 7) Open comedones (White head) 8)Close comedones (black heads) 9) Papule 10)Pustule. 11)Nodules.

Exclusion Criteria

  • Patient suffering from any other skin disease and any allergic condition.
  • Patients of severe acne having inflammatory cyst.
  • Genetic disorders.

Outcomes

Primary Outcomes

Prepare Sahachara Ghrita and its cream form, to study its organoleptic, physio-chemical, phyto-chemical parameters and clinically compare its effect with Shalmali Kantaka Lepa on Mukhadushika.

Time Frame: Follow up 0th,15th,30th,and 45th day.

Secondary Outcomes

  • Not applicable(not applicable)

Investigators

Sponsor
Dr Manjusha Suresh Uikey
Sponsor Class
Other [[self]]
Responsible Party
Principal Investigator
Principal Investigator

Dr Manjusha Suresh Uikey

Shri Ayurved Mahavidyalaya, Nagpur

Study Sites (1)

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