Tackling Dry Socket Via Laser Therapy in Smokers | NCT06481293

Studies
Tackling Dry Socket Via Laser Therapy in Smokers

NCT06481293

Sponsor

Badr University

Status

Completed

Last Update Posted

Sep 25, 2025Actual

Enrollment

50Actual

Phase

Not Applicable

Conditions

Alveolar Osteitis

Interventions

Diode laser therapy
Alveogyl dressing

Countries

Egypt

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Sep 2025

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Oct 30, 2023Actual

Primary Completion Date

Sep 20, 2024Actual

Completion Date

Sep 20, 2025Actual

First Submitted Date

Jun 25, 2024

First Submission Date that Met QC Criteria

Jun 25, 2024

First Posted Date

Jul 1, 2024Actual

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Sep 21, 2025

Last Update Posted Date

Sep 25, 2025Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Not provided

Is FDA Regulated Drug

Is FDA Regulated Device

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

This study examines the efficiency of diode laser therapy to manage dry sockets after tooth extraction.

Detailed Description

The study compares the efficiency of diode laser therapy and using only alveogyl to accelerate the healing of dry sockets after tooth extraction in smokers. Smoker patients with dry sockets were enrolled randomly into two different groups. Group 1 received dual wavelength laser diode therapy, three times per week. While group 2 received only a topical application of alveogl. The treatment lasted for two consecutive weeks. The treatment efficiency was evaluated by measuring the volume of the socket using the syringe method. The pain level was measured by the visual analog scale.

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

50Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Group 1	Experimental	Group 1 received diode laser therapy	Device: Diode laser therapy
group 2	Experimental	Group 2 received topical application of aveogl dressing	Combination Product: Alveogyl dressing

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Diode laser therapy	Device	Dual wavelength laser diode therapy device	Group 1

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Socket volume	measured through the volumetric measurement method using a syringe filled with saline	2 weeks

Secondary Outcomes

Measure	Description	Time Frame
Pain level	measured by the visual analogue scale(VAS). It include score from 0 to 10 in which 10 indicates the worst pain level and 0 indicates no pain	2 weeks

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Smokers patient

Exclusion Criteria:

Females on contraceptives.
Diabetic patients
Hepatitis C virus patients
Patients on corticosteroids
Patients with renal diseases
Anemic patients

Accepts Healthy Volunteers

Yes

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

25 Years

Maximum Age

40 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Name	Affiliation	Role
reham Elkalla, lecturer	Badr University in Cairo	Principal Investigator

Locations

Facility	Status	City	State	ZIP	Country	Contacts
Badr University in Cairo		Cairo		11837	Egypt

IPD Sharing Statement Module

Plan to Share IPD

Description

Not provided

Types

Not provided

Time Frame

Not provided

Access Criteria

Not provided

URL

Not provided

Condition Browse Module

MeSH Terms

ID	Term
D004368	Dry Socket

Ancestor Terms

ID	Term
D009059	Mouth Diseases
D009057	Stomatognathic Diseases

Browse Leaves

Not provided

Browse Branches

Not provided