Low-Level Laser Therapy vs. Saline for Wound Healing After Primary Molar Extraction.

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-10-31

Study Completion Date

2026-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To evaluate the effect of low level laser therapy versus the saline on wound healing after extraction of primary Molars

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Low Laser Light Therapy After Impacted Third Molar Removal

NCT02602431

Trismus Edema Pain

UNKNOWN NA

Evaluation of the Remineralizing Effect of Aloe Vera Versus Diode Laser for Management of Deep Carious Lesions.

NCT05327049

Deep Caries

COMPLETED NA

Effect of Diode Laser on Sensitive NCCLs Prior to Composite Restoration, Dentin Bonding, and Clinical Durability of Composite Restorations.

NCT05501691

Dentin Hypersensitivity

COMPLETED NA

Comparison of LASER Therapy and Desensitizing Agents in Dentinal Hypersensitivity

NCT06759454

Dentinal Hypersensitivity

NOT_YET_RECRUITING NA

Clinical Study of Biostimulation With Low-Power Diode Laser After Dental Extractions

NCT06943391

Laser Therapy, Low-Level

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Wound-healing

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Low-level laser therapy

Effect of Low-level laser therapy in wound healing after primary molar extraction

Group Type EXPERIMENTAL

Low-level laser

Intervention Type DEVICE

Effect of Low-level laser therapy in wound healing after primary molar extraction

Saline

Normal saline in wound healing after primary molar extraction

Group Type ACTIVE_COMPARATOR

Saline Solution (NaCl 0,9%)

Intervention Type OTHER

Following the extraction, a piece of gauze soaked in normal saline solution (NSS) will be placed over the socket. Both parents and children will be instructed to keep the gauze in place for 45 minutes

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Low-level laser

Effect of Low-level laser therapy in wound healing after primary molar extraction

Intervention Type DEVICE

Saline Solution (NaCl 0,9%)

Following the extraction, a piece of gauze soaked in normal saline solution (NSS) will be placed over the socket. Both parents and children will be instructed to keep the gauze in place for 45 minutes

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* ● Children aged from 4 to 6 years.

* Children of both genders.
* Medically fit ASA I.
* Children with badly decayed primary molars beyond repair and indicated for extraction.
* Parents acceptance to participate in the study.
* Cooperative children.
* Antibiotics and painkillers have been stopped at least 12 hours prior to the procedure.(Özer et al., 2024)
* Teeth with at least two-thirds of the root.

Exclusion Criteria

* ● Uncooperative children.

* Lack of informed consent by the child patient's parent to be approved ethically.
* Unable to attend follow-up visits to avoid attrition bias by decreasing the number of drop off cases.
* Medical history includes conditions such as prolonged bleeding, platelet disorders, hypersensitivity, allergic reactions to pain relievers, contraindications to laser therapy, and acute pain.
* Teeth with root lengths less than two-third of the normal root length or those who experienced extensive iatrogenic trauma during tooth extraction.

Minimum Eligible Age

4 Years

Maximum Eligible Age

6 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes