Combination Therapy Effect of Laser on Wound Healing and Bone Regeneration of Dental Sockets
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Diode Laser 980 nm..
- Who it may be relevant to
- Registry conditions: Tooth Extraction. Basic parameters: from 21 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Pakistan
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The goal of this clinical trial is to learn if the laser works to improve wound healing and bone regeneration after tooth extraction. The main question it aims to answer is: Does laser therapy improve wound healing and bone regeneration after tooth extraction? Researchers will compare a laser to sham laser therapy to see if the laser enhances wound healing and bone regeneration. Participants will: Have exposure to laser or sham laser therapy immediately after tooth extraction Record their pain intensity on days 2, 4, 6 and 14 Visit the clinic after 10 days for follow-up Again, visit the clinic after 4 months for evaluation
Interventions
- Other Diode Laser 980 nm.
A Diode laser is commonly used in simple surgical procedures on soft tissue, such as skin or mucosa. Its tip can work when non-activated, causing inductive effects, and when activated, it causes the ablation of soft tissue.
Primary outcome measures
- Wound healing will be assessed in both the experimental and control groups. [Time frame: 1 year]
- Bone regeneration will be assessed in both the experimental and control groups. [Time frame: 1 year]
Secondary outcome measures (1)
- Pain intensity will be measured in both the experimental and control groups. [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
- At least 21 years old, regardless of gender
- Non-traumatic tooth extraction of the lower jaw is indicated
- Willing for dental implant surgery
- Dental appointments are available at the study place
- Absence of active infection at the extraction site
- Signed informed permission is provided.
Exclusion criteria
- Pregnant, lactating, and menopausal women
- Smokers
- Those having head and neck radiotherapy
- Those with any sort of acute infection (e.g., periodontal abscess), immune deficiency, or metabolic conditions such as diabetes mellitus and osteoporosis
- Patients will also be eliminated if they have a complication during surgery, such as bleeding or operational difficulties, or if the procedure takes longer than 90 minutes.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Supportive care
Study locations
Pakistan · 2 centers
- Sharif Medical and Dental College — Lahore
- Sharif Medical and Dental College — Lahore
Identifiers
NCT: NCT06552936 · SMDC/SMRC/242-22