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A Comparative Single Blind Clinical Study on the Effect of Alvogyl, Eugenol, and Nigella Sativa (Black Seed Oil) for Alveolar Osteitis.

ConditionAlveolar Osteitis
Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age16-70
SponsorHITEC-Institute of Medical Sciences

About this trial

Dry socket the unscientific term also known as alveolar or fibrinolytic osteitis is the most common postoperative complication following tooth extraction.

Treatment of Alveolar osteitis can be either pharmacological on non-pharmacological. Management can be by irrigation, surgical intervention and placement of medicated dressing such as topical anti-bacterial, topical anesthetics and obtundants or combination of these three.this study aims to find the best and effective treatment for dry socket comparing Alveogyl, Eugenol and Black seed oil at this institution.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over the age of 16, from both genders, who had their teeth extracted and were clinically diagnosed with dry socket.

Absence of systematic disease.

Disqualifiers

SMOKER

ALCOHOLIC

Patients under the age of 16 years and over the age of 70 years

Patient with various bone diseases including osteoporosis.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Alvogyl

    Drug

    this is standard treatment drug

  • Eugenol

    Drug

    this not standard drug for the treatment of Alveolar Osteitis but an antiseptic agent

  • Nigella Sativa Oil

    Drug

    it not standard medicine for Alveolar Osteitis. it is a herbal medicine

Treatment groups

40 Participants
are divided into 3 treatment groups
Group A: AlvogylExperimental treatment 1 intervention
Group B: EugenolExperimental treatment 1 intervention
Group C: Black Seed OilExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Visual Analogue Scale

pain will assessed using Visual Analogue scale on day 2, 6, 10 and 14th after the start of treatment. Visual Analogue Score measurement will be scale based from 1 to 10 score. Where 1-3 is mild, 3-7 is moderate and 7-10 will be scored as severe pain.

Time frame
14 days
2

Periodontal Probe

alveolar osteitis affected extraction socket will be observed for the resolution of inflammation and healing will be assessed on day 2, 6, 10 and 14 by clinical examination with periodontal Probe. Periodontal depth will be measured in mm, by using the periodontal probe where the depth of 1 to 3 mm is considered well healed socket, 4-6 mm indicates moderately inflamed, 7 mm and above is considered severely inflammed .

Time frame
14 days

Secondary outcomes

Other outcomes

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Department of Oral & Maxillofacial Surgery-Dental College HITEC-IMS TAXILA CANTT Status unavailable 47070, Taxila Cantt, Punjab ProvincePakistanPakistan

Sponsors and contacts

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

HITEC-Institute of Medical Sciences

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: