Photo Biomodulation Therapy for Alveolar Osteitis Recovery in Oral Contraceptive Users

N/ACompletedNCT06865508

Badr University50 enrolled

Overview

does laser effect on alveolar osteitis recovery in oral contraceptive users ?

photo biomodulation therapy for alveolar osteitis recovery in oral contraceptive users

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Alveolar Osteitis

Interventions

Laser therapyDEVICE

Laser therapy was administered using a low-level laser device with the following parameters: \[ wavelength 980 nm810, power 500mw, and duration 90 seconds (30second for each 3 sides\].

zinc oxide eugenol dressing.DEVICE

zinc oxide eugenol dressing.

Eligibility

Sex: FEMALEMin age: 25 YearsMax age: 40 Years

Medical Language ↔ Plain English

* Inclusion Criteria: Female patients aged 25-40 years. Currently using oral contraceptives for at least 3 months prior to participation. Diagnosed with dry socket (alveolar osteitis) based on clinical criteria. * Exclusion Criteria: Presence of systemic diseases (e.g., diabetes, immunodeficiency disorders). Smoking or tobacco use. Allergies to zinc oxide or other study materials. Use of antibiotics or anti-inflammatory medications within the last 2 weeks. Pregnancy or breastfeeding.

Locations (1)

physical therapy at Badr University in Cairo(BUC)

Cairo, Egypt

Outcomes

Primary Outcomes

pain intensity by VAS

Pain intensity measured using a Visual Analog Scale (VAS) at day0, day7, day14 post-treatment.

Time frame: 4 weeks

Socket volume .

measured using \[specific measurement technique, volumetric analysis\] at day0, day14 and 1-month post-treatment

Time frame: 4 weeks

Secondary Outcomes

Quality of life assessed

Quality of life assessed using the Oral Health Impact Profile (OHIP-5) questionnaire at day0, day7and day14 post-treatment.

Time frame: 4 weeks

Data from ClinicalTrials.gov

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