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Third molar removal surgeries included: comparison of the use of high and low level lasers

Clinical evaluation of signs and symptoms of patients submitted to different inflammation control protocols in third molars removal surgery: a randomized, controlled, double-blind trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-4qgtmyw
Enrollment
Unknown
Registered
2021-05-17
Start date
2019-06-05
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Anomalies of tooth position

Interventions

There will be 84 patients, who will be allocated to one of the 06 subgroups, with 14 in each subgroup. Patients will be divided into 3 groups (A, B and C) according to the strategy to control inflamma
E02.594
VS2.002.001

Sponsors

Instituto Para O Desenvolvimento Da Educacao Ltda - IPADE
Lead Sponsor
Centro Universitário Christus
Collaborator

Eligibility

Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: Healthy volunteers; Both genres; non smokers; age between 18 and 30 years; In need of removal of the four semi-inclusion or inclusion (not erupted in the mouth) in any inclination ratio with the distal face of the second molar, with the proximity of the branch of the jaw and in any depth.

Exclusion criteria

Exclusion criteria: Volunteers smokers; History of alcohol or drug abuse; pregnant women, lactating or in the use of contraceptives; which have referred to some systemic disease; which make use of some chronic use medication; which have used any medication with anti-inflammatory effect during the last 30 days; which present chronic pain or neurological disorder; which have used in the last 15 days some bifosphonate medication, which have submitted pericoronaritis in the last month; which have a history of photosensitivity or reporting allergy to any of the drugs used in the survey.

Design outcomes

Primary

MeasureTime frame
To evaluate mean differences in clinical parameters related to inflammatory events (pain).

Secondary

MeasureTime frame
To evaluate mean differences in clinical parameters related to inflammatory events (edema and trismus).

Countries

Brazil

Contacts

Public ContactCaio Vinicius G. Roman torres
cvgrt@hotmail.com1121518603

Outcome results

None listed

Source: REBEC (via WHO ICTRP)