Pain, swelling and healing following surgical extraction of symmetrical impacted lower third molars Oral Health
Conditions
Interventions
This study is a split mouth randomized clinical trial. Both chamomile gel and placebo gel were colored red and loaded in coded syringes ("A" and "B") in equal quantities (2 ml), the researcher and the
Sponsors
Damascus University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Age 18-28 years 2. Indication for surgical extraction of impacted lower third molars in a symmetrical position according to the classification of Pell & Gregory 3. Good general health and there are no uncontrolled systemic diseases 4. Good oral health 5. No previous pain 6. No allergy or contraindication to the required postoperative prescription or to the Plants of Asteraceae/compositae family
Exclusion criteria
Exclusion criteria: 1. Pregnancy or current menstraution 2. Uncontrolled diabetes, uncontrolled hypertension, neoplasms, known neuropsychiatric illness, blood dyscrasia, coagulation disorders, or metabolic disorders 3. Compromised immune system or other systemic diseases 4. Patients with pericoronitis, infection, pathological condition in the region of surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| At 3 and 7 days. 1. Pain measured using visual analogue scales (VAS) 2. Facial swelling (clinical evaluation) 3. Mouth opening (clinical evaluation) 4. Soft tissue healing (clinical evaluation) | — |
Secondary
| Measure | Time frame |
|---|---|
| There are no secondary outcome measures | — |
Countries
Syria
Outcome results
None listed