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Investigating the effect of laser in the treatment of dry socket

Investigating the effect of low level laser therapy on pain in patients with dry socket in comparison to the conventional method

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015051722299N1
Enrollment
16
Registered
2015-06-27
Start date
2015-06-05
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. Alveolar osteitis

Interventions

Intervention 1: In the intervention group, the patients are irradiated with a low level laser in a "continuous Mode" with a wavelength of 808 nm and a power of 100 mW. Laser is radiated for 60 seconds
Treatment - Devices
Treatment - Drugs
In control group, the extraction area is wash out with sterile Salin solution and cover with Zinc Oxide Eugenol pack. This treatment is repeated up to three sessions and every other day.
In the intervention group, the patients are irradiated with a low level laser in a "continuous Mode" with a wavelength of 808 nm and a power of 100 mW. Laser is radiated for 60 seconds with a distance

Sponsors

Vice Chancellor for research of Faculty of Dentistry at Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria is the previous diagnosis of dry socket without taking any previous treatment. The criteria for the diagnosis of dry socket is the pain after tooth extraction in the extraction area and around it which is growing in next three days and is along with the full or partial breakdown of clots. Items that are excluded from the study include the past history of radiation therapy, any medical problem that may affect the treatment of dry socket (such as the pathological state of bone, vascular and hematologic diseases and diabetes mellitus),and the use of antibiotics, pregnancy and breast-feeding. Also, patients who smoke, who are in the menstrual cycle and those who take oral contraceptive medicines.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before the treatment, before and after each treatment session, which takes place every other day. Method of measurement: VAS (Visual Analogue Scale).

Secondary

MeasureTime frame
The number of analgesic tablets. Timepoint: Before the treatment and after each treatment session, which takes place every other day. Method of measurement: The number of tablets consumed is calculated according to the questionnaire filled out by the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElaheh Aghababarangraz

Faculty of Dentistry at Tehran University of Medical Sciences

E-rangraz@student.tums.ac.ir+98 21 8801 5950

Outcome results

None listed

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