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Clinical Trials/CTRI/2025/07/090680
CTRI/2025/07/090680RecruitingNot Applicable

Comparative Clinical Study of Navakarshika Guggulu and Haridrakhanda in Sheetpitta (Urticaria)

Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan1 site in 1 country60 target enrollmentStarted: July 21, 2025Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
60
Locations
1
Primary Endpoint
is assessed

Study Overview

Brief Summary

This study is an open label, double arm comparative study, comparing the efficacay of Navakarshika Guggulu 500mg twice daily after meal and Haridrakhanda 4 gm twice daily before meal in 60 patients with sheetpitta(urticaria) that will be conducted in Opd no. 13/14 iin Patanjali Ayurveda Hospital, Haridwar. Assessment will be done on the basis of subjective and objective parameters.

Route of administrarion- Oral route

Follow up- will be done to observe effects of treatment or any adverse effect on the patient.

1st follow up- 1 month after commencement of tratment

2nd follow up- 1 month after the 1st follow.

Study Design

Study Type
Interventional
Allocation
Na
Masking
None

Eligibility Criteria

Ages
16.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients willing to participate.
  • Patients with classical symptoms of urticaria.
  • Patients will be selected irrespective of gender and socio economic status.

Exclusion Criteria

  • Patient having any systemic illness like tuberculosis, carcinoma and endocrine disorders or any major illness like renal or liver disorder.
  • Pregnant and lactating woman.
  • Patients consuming steroids on regular basis for any ailment.

Outcomes

Primary Outcomes

is assessed

Time Frame: 0day 30days 60days

Subjective parameters- Grading will be done considering signs and symptoms of sheetpitta-

Time Frame: 0day 30days 60days

1. Kotha (Raised skin,lesions,rashes)

Time Frame: 0day 30days 60days

2. Kandu (Itching sensation)

Time Frame: 0day 30days 60days

3. Toda (Pricking pain)

Time Frame: 0day 30days 60days

4. Daha (Burning sensation)

Time Frame: 0day 30days 60days

Objective Parameters-

Time Frame: 0day 30days 60days

1. No. of wheals

Time Frame: 0day 30days 60days

2. Intensityof pruritis

Time Frame: 0day 30days 60days

3. Duration of wheals

Time Frame: 0day 30days 60days

4. Freq. of appearance

Time Frame: 0day 30days 60days

5. Freq. of histamines

Time Frame: 0day 30days 60days

Secondary Outcomes

  • Subjective parameters- Grading will be done considering signs and symptoms of sheetpitta-(1. Kotha (Raised skin,lesions,rashes))

Investigators

Sponsor
Patanjali Bhartiya Ayurvigyan Evam Anusandhan Sansthan
Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Udita Kuria

Patanjali Bharatiya Ayurvigan Evam Anusandhan Sansthan

Study Sites (1)

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