Comparison Of Saliva PH Before And After Consumption Of Licorice Product, A Controlled Clinical Trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190314043054N1

Enrollment

Registered

2019-06-12

Start date

2019-01-30

Completion date

Unknown

Last updated

2019-08-26

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

Conditions

Changes in salivary PH-Licorice.

Interventions

Intervention 1: Intervention group: Tablet D-REGLIS, production of Iran DAROUK Company with drug registration number of 1228104305-These pills contain 380 mg of dried and standardized extracts of lic

Eligibility

Sex/Gender

All

Age

20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. Informed consent 2-age between 20 to 40 years 3-Weight between 56 to 80 kg 4-Not taking the drug one month before the sampling

Exclusion criteria

Exclusion criteria: 1-allergy to licorice 2-pregnancy 3-Developing systemic disease 4- addiction to cigarettes 5- History of dry mouth

Design outcomes

Primary

Measure	Time frame
PH of Saliva. Timepoint: Before the intervention/20,40,60,90,120,180 minutes after the intervention. Method of measurement: PH Meter device-INOLAB 720-made in Germany.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohsen Vosough

Bojnourd University of Medical Sciences

javad.snm68@gmail.com+98 58 3635 7638

Outcome results

None listed

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