Effectiveness of Artificial Saliva in improving dry mouth and quality of life among the elderly

Effectiveness of Different Saliva Substitutes in improving the Oral Health related Quality of Life among the elderly- A Randomized Controlled Trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2021/01/030436

Enrollment

Registered

2021-01-13

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: K110- Atrophy of salivary gland

Interventions

Intervention1: ICPA Wet Mouth mouthrinse: Composition: Sodium Carboxymethyl Cellulose 0.5% w/v,Glycerine 30%w/v, Flavoured base Dose:10 ml Frequency:3 times a day Route of administration: Topical(mout

Eligibility

Inclusion criteria

Inclusion criteria: Adults aged >=60 years, who are under at least 2 prescription medications for a year or more and unstimulated salivary flow rate <= 0.25 ml/min

Exclusion criteria

Exclusion criteria: Patients with a history of Sjogrenâ??s syndrome, Salivary gland infection, Irradiated Head and neck cancer patients, History of total or partial removal of Salivary glands, Participant who is not willing to sign the informed consent.

Design outcomes

Primary

Measure	Time frame
XerostomiaTimepoint: 2 months after intervention	—

Secondary

Measure	Time frame
oral health related quality of lifeTimepoint: 2 months after intervention	—

Countries

India

Contacts

Public ContactAthira Purushothaman

Yenepoya Dental College

merekhap@gmail.com9845132999

Outcome results

None listed

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