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Evaluation of side effects of two types of flap after impacted mandinular third molar surgery

The effect of two types of envelope and modified triangular flap in the prevention of dry socket after mandibular third molar surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014052717863N2
Enrollment
60
Registered
2014-06-17
Start date
2013-06-30
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

dry socket. Alveolitis of jaws

Interventions

Intervention 1: In an intervention group,modified triangular flap was used the presence of dry socket was evaluated after 7 days from the surgery. Intervention 2: In a control group,modified triangula
Treatment - Surgery
In an intervention group,modified triangular flap was used the presence of dry socket was evaluated after 7 days from the surgery.
In a control group,modified triangular flap was used the presence of dry socket was evaluated after 7 days from the surgery

Sponsors

Shahid Sadoughi University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 34 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: bilateral impacted mandibular third molar teeth with equal location in the jaw; no associated pathology; the plaque index score lower than 20%; no use of any antibiotics or anti-inflammatory drugs within 14 days before surgery; root formation between 1/3to 2/3. Exclusion criteria: Patients with a history of systemic disease; pregnancy; milking period or a history of dry socket; deep bony impaction of lower third molars; poor oral hygiene; recent history of pericoronitis; ulcerative gingivitis or active infection associated with the extracted tooth; smoking; oral contraceptive tablet use and immunocompromised patients.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Dry socket. Timepoint: after seven days. Method of measurement: clinical.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSahebe Talebi Banizi

Shahid Sadoughi University of Medical Sciences

talebi.sahebe@yahoo.com sahebetalebi@ssu.ac.ir+98 35 1825 2484

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026