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Topical Analgesic Versus Saline Mouth Rinses in Post Extraction Healing

Comparison of Topical Analgesic With Saline Rinses in Post Extraction Healing Among Hypertensive and Non-Hypertensive Patients

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03130153
Enrollment
60
Registered
2017-04-26
Start date
2016-01-01
Completion date
2017-12-31
Last updated
2018-06-28

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

Conditions

Tooth Extraction Site Healing

Brief summary

There is no evidence based guidelines on using saline rinses for post extraction oral care among hypertensives. Similarly, benefit of orally dissolved topical analgesics in addition to orally administered analgesic is questionable.

Detailed description

Objective: To compare the post dental extraction healing among subjects who took simple analgesic tablets dissolved in water versus those who used saline rinses post operatively. Methods: A study will be done among patients who underwent dental extractions at AKHSP dental clinic, Karachi, Pakistan. Carious, periodontally mobile, traumatized or broken down teeth among 20-70 years old in either gender will be included. In addition to the routine prescription of antibiotics and oral analgesics, the hypertensive subjects (n=20) will be advised to take dissolved Aspirin tablet as an oral care while non-hypertensive will be divided into two sub groups (n=20 each), advised saline mouth rinses or dissolved Aspirin for 5 days, respectively. The outcome (healing of the extraction socket) will be evaluated 7 days from the day of extraction on an ordinal scale.

Interventions

DRUGAspirin Powder

Aspirin powder to be dissolved in water and to be used as mouthwash twice daily for 7 days after tooth extraction.

DRUGNormal saline

Normal saline to be used as mouthwash twice daily for 7 days after tooth extraction among non-hypertensive subjects.

Sponsors

Aga Khan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Carious, periodontally mobile, traumatized or broken down teeth needing extraction * Age 20-70 years, both genders

Exclusion criteria

* Diabetes * Osteoporosis, metabolic bone disease etc. * Radiation therapy or chemotherapy.

Design outcomes

Primary

MeasureTime frameDescription
Healing of the extraction socketSeven days from the day of extraction1. = healed or healing well 2. = incomplete healing but progressing 3. = poorly healed open margins and readily bleeding

Countries

Pakistan

Outcome results

None listed

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