Efficacy of a Potassium Nitrate Containing Herbal Mouthwash to a Potassium Oxalate Mouthwash in Dentinal Hypersensitivity

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-60
SponsorDr. D. Y. Patil Dental College & Hospital

About this trial

The goal of this clinical trial is to compare the efficacy of potassium nitrate containing herbal mouthwash to potassium oxalate mouthwash in management of dentinal hypersensitivity.

* Participants will be divided into two groups by computer generated randomization. The participants will be divided into two groups, Group 'A' and Group 'B' by Simple Random Allocation as both groups, each group will involve 20 participants with at least two sites showing dentinal hypersensitivity * The assessment of Dentinal Hypersensitivity will be done after scaling and/or root planing (if required) by subjecting affected sites with Air Blast Test (ABT), Cold Water Test (CWT) and Tactile Response assessment will be recorded using Visual Analogue Scale (VAS). All sensitivity tests will be executed by a single examiner who will be blinded to the randomization and will record DH at baseline and at 4, 8 and 12 weeks

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participants with at least two DH sites with VAS score ≥4

Participants with teeth showing cervical abrasion, erosion, gingival recession

Participants >18 years in general good health

Participants self-reporting with history of dentinal hypersensitivity to various stimuli.

Disqualifiers

Teeth with severe caries, faulty restoration, prosthetic crown, chipping, fracture, symptoms of pulpal damage

Participants who has taken long term analgesic therapy within 30 days before the start of the study

Participants who have undergone any treatment for dentinal hypersensitivity in past 3 months

Participants with ongoing orthodontic therapy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Mouthwash preparation

    Drug

    Participants will be divided into two groups Group A and Group B Both the groups will receive thorough scaling and root planing at required sites. Use of mouthwash preparation is adviced for 8 weeks and discontinue after for 4 weeks. The Visual analogue scale Hypersensitivity will be assessed via Visual Analogue Scale at 4, 8 and 12 week interval

Treatment groups

40 Participants
are divided into 2 treatment groups
Group A: Potassium nitrate containing herbal mouthwashExperimental treatment 1 intervention
Group B: Potassium oxalate mouthwashActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Dentinal Hypersensitivity

The dentinal hypersensitivity will be assessed using Visual Analogue Scale

Time frame
at 4, 8 and 12 week interval

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dr. D. Y. Patil Dental College & Hospital

Lead sponsor

Jasberry Healthcare Pvt. Ltd

Collaborator