Skip to content

Role of Triphala Kwath Abhyantar Prayog with Triphala Kwath Gandusha in the treatment of Mukhapaka in the age group of 18 to 60 years.

A standard controlled clinical trial on Triphala Kwath Gandusha with and without Triphala Kwath Abhyantar Prayoga in Mukhapaka

Status
Active, not recruiting
Phases
Phase 1Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/05/019288
Enrollment
60
Registered
2019-05-23
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K121- Other forms of stomatitis

Interventions

Intervention1: Triphala Kwatha Abhyantar Prayog and Triphala Kwath Gandusha: 1pala ( 48gms) of Triphala choorna is to be taken. Sixteen part of water is added to the choorna. This entire mixture is th

Sponsors

PDEAs College Of Ayurveda and Research center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having signs and symptoms of Mukhapaka(Sarvasara) I) AsyaVrana. II) AsyaRuja. III) AsyaDaha. IV) AsyaVairasyata. V) JihvaSfutana 2. Patients having age between 18-60 yrs. 3. Chronicity of Mukhapaka less than 1 year. 4. Recurrent oral ulcer with symtoms of Mukhapaka .

Exclusion criteria

Exclusion criteria: 1. Agantuja Mukhapaka(traumatic etc.) 2. Known case of AIDS, oral cancer and diabetes mellitus. 3. Patients recently undergone oral surgeries (history of surgery done in last 6 months).

Design outcomes

Primary

MeasureTime frame
To study the comparison between the effect of Triphala Kwath Gandusha with and without Triphala Kwath Abhyantar Prayoga for the period of 1 month in the effective management of Mukhapaka.Timepoint: 1 month

Secondary

MeasureTime frame
To observe the side effects during the study if any.Timepoint: 30 days

Countries

India

Contacts

Public ContactDr Pratima Kale

PDEAs College of Ayurveda and Research center

virkar.chandana@gmail.com9822199107

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026