Efficacy of Azadirachta Indica Based Herbal Mouthwash in Treating the Tooth Hypersensitivity

Clinical Efficacy of Azadirachta Indica Based Herbal Mouthwash in Treating the Hypersensitivity of Teeth

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06288776

Enrollment

120

Registered

2024-03-01

Start date

2023-02-01

Completion date

2023-04-30

Last updated

2024-03-01

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

Conditions

Tooth Sensitivity

Keywords

Azadirachta indica, Gingival Index, Herbal, Mouthwash, Tooth sensitivity

Brief summary

Type of study: Single-blinded clinical trial to evaluate the effectiveness of Azadirachta indica based Herbal mouthwash to treat the tooth sensitivity in patients. Participants aged 20 years and above having Gingival Index score 3 will be included in the study. Their tooth sensitivity will be checked initially and then they will be given Herbal based mouthwash for 3 months. Again, their tooth sensitivity shall be checked after 3 months.

Detailed description

In this study Herbal based mouthwash will be evaluated for eliminating the tooth sensitivity in the participants having Gingival Index score 3 with VAS scores for sensitivity ranging between 30-80 . Consecutive non-random sampling technique will be used in this study where Participants included will be assessed for tooth sensitivity through Visual Analogue Scale (VAS) initially for base line readings. These participants will be given Azadirachta indica based Herbal mouthwash for three months and then again their tooth sensitivity will be assessed by Visual Analogue Scale (VAS) for final readings. The mean values of VAS scoring both before and after the usage of herbal mouth wash will be compared to investigate the clinical efficacy of this mouthwash in treating the tooth sensitivity.

Interventions

DIAGNOSTIC_TESTHerbal based mouthwash

Herbal based mouthwash will be used to treat the tooth sensitivity in participants having VAS score values of tooth sensitivity ranging between 30-80

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Masking description

Single-blinded study where participant will be masked.

Intervention model description

In this study, participants will be selected by consecutive non-random sampling technique.

Eligibility

Sex/Gender

ALL

Age

20 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Patients with good general health and no allergy * Patients who have not used any mouthwash in last 3 month * Study teeth shall be free of decay and restoration * Study teeth shalll not be mobile * Study teeth shall have the Gingival Index score 3 * Participants shall be able to read ,write and willing to give consent.

Exclusion criteria

* Patients with poor general health and allergies * Patients who have used any mouthwash in last 3 months * Teeth with decay and restorations * Teeth with mobility * Teeth with Gingival Index score more than 3 * Participants that wonn't be able to read ,write and willing to give consent.

Design outcomes

Primary

Measure	Time frame	Description
Toothsensitivity declination with herbal based mouthwash	3 months	Evaluation of herbal based mouth wash in eliminating the tooth sensitivity ranging between VAS scores 30-80.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026