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Clinical Trials/CTRI/2025/02/081281
CTRI/2025/02/081281
Not yet recruiting
Phase 2/3

A randomised comparative clinical study on the effect of hutabugadi choorna and murvadi choorna in pandu.

Dr Pallavi S1 site in 1 country60 target enrollmentStarted: March 8, 2025Last updated:

Overview

Phase
Phase 2/3
Status
Not yet recruiting
Sponsor
Dr Pallavi S
Enrollment
60
Locations
1
Primary Endpoint
Srama/Fatigue

Overview

Brief Summary

This is a randomized comparative clinical study to evaluate the effect of hutabugadi choorna and moorvadi choorna in management of symptoms of pandu for 30 days this study comprises of two groups of 30 patients seected as inclusion and exclusion criteria study will be conducted in ALN Rao memorial ayurvedic hospitals in koppa koppa taluk chikmaglur 577126 karnataka India.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • 1.Subjects with the lakshanas of panduta, dourbalya, hataanila, srama, bhrama, and hrutspandana, of pandu.
  • 2.Hb percentage more than 8 gmpercent & less than 13gmpercent in male, less than 12gm percent in females.
  • 3.Subjects above the age of 18 years and below 60 years irrespective of caste, gender, religion and socio-economic status.
  • 4.Subjects must be capable of giving informed consent, willingness and ability to comply with scheduled visits, treatment plans and laboratory tests and other study procedure.

Exclusion Criteria

  • 1.Patients with uncontrolled systemic diseases like Diabetes Mellitus and Hypertension.
  • 2.Endocrine disorders like hypothyroidism, Cushing syndrome, etc.
  • 3.Patient having tuberculosis, known case of HIV, leprosy, any type of Cancer.
  • 4.Patients with infectious diseases such as chickenpox, dengue etc.
  • 5.Haemoglobinopathies such as Sickle cell anaemia, Leukaemia and Thalassaemia.
  • Pregnant and lactating women 7.Patients with active bleeding disorders like Haemorrhoids, menorrhagia, gastro intestinal bleeding.
  • 8.Anaemia in a case of defective absorption due to gastrectomy, sprue syndrome etc.

Outcomes

Primary Outcomes

Srama/Fatigue

Time Frame: 30 days

Bhrama/Giddiness

Time Frame: 30 days

Hrutspandana/Palpitations

Time Frame: 30 days

Panduta of Tvaka, Nakha, Netravartma, Jihva, Hastapadatala/Paleness of skin,eye,tongue,foot and palm.

Time Frame: 30 days

Dourbalya/Generalised weakness

Time Frame: 30 days

Hataanila/Reduction of digestive fire

Time Frame: 30 days

Secondary Outcomes

  • Not applicable(Not applicable)

Investigators

Sponsor
Dr Pallavi S
Sponsor Class
Other [self]
Responsible Party
Principal Investigator
Principal Investigator

Dr Pallavi S

ALN Rao Memorial Ayurvedic Medical College Koppa Chikkamagaluru Karnataka India

Study Sites (1)

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