Skip to main content
Clinical Trials/NCT04353999
NCT04353999CompletedNot Applicable

The Effect of Diode Laser Photocoagulation on the Soft Tissue Healing During Socket Preservation in the Esthetic Zone.

Hams Hamed Abdelrahman1 site in 1 country36 target enrollmentStarted: March 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
36
Locations
1
Primary Endpoint
Soft tissue healing (the changes in the soft tissue color throughout the first month)

Study Overview

Brief Summary

The main aim of this study was to evaluate clinically the effect of laser photocoagulation in comparison to the non-resorbable dense polytetrafluroethylene (dPTFE) membrane on the soft tissue healing during socket preservation with bovine bone xenograft.

Detailed Description

The study was designed as randomized, controlled, clinical trial. patients who were undergoing tooth extraction and socket preservation were divided into two groups: Group I:980 nm Diode laser was used to seal the socket by photocoagulation .Group II : a non-resorbable dPTFE was used to seal the socket and stabilized by suturing to the soft tissue margins of the socket

All patients were clinically and radiographically evaluated at the baseline and on the second , third and fourth weeks postoperatively.Then recalled after 4 months for the final radiographic examination.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Triple (Participant, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •The need for the extraction of nonrestorable maxillary anterior tooth for untreatable caries, endodontic treatment failure or root fracture.
  • •Type I postextraction sockets according to the classification proposed by Elian et al. with all bony walls intact .
  • •Adult patients (aged 18-50 years).
  • •A good standard of oral hygiene, as determined by the registration of an O'Leary Plaque Index of less than or equal to 10% after phase I therapy.

Exclusion Criteria

  • •The presence of any systemic disease that could complicate bone and soft tissue healing of the grafted socket.
  • •The presence of any local factor that may interfere with extraction as tooth ankylosis.
  • •The presence of bone dehiscence and fenestrations of the post-extractive alveolus (Type II and III sockets).
  • •Subjects who had undergone radiation therapy.
  • •Patients who had been subjected to or who were under bisphosphonate therapy.

Arms & Interventions

980 nm diode laser photocoagulation

Experimental

980 nm diode laser was used to coagulate the blood over the bone graft particles and achieve a socket seal after socket grafting

Intervention: Socket sealing by diode laser photocoagulation (Procedure)

Dense polytetrafluroethylene membrane

Active Comparator

dPTFE membrane was used to seal the socket after grafting

Intervention: socket sealing with dense polytetrafluroethylene membrane (Procedure)

Outcomes

Primary Outcomes

Soft tissue healing (the changes in the soft tissue color throughout the first month)

Time Frame: at 2nd, 3rd and 4th week

clinical examination and scoring according to Landry healing index. A score of 1 to 5 was given to the surgical site indicating the improvement of the nature of the soft tissue . A score of 1 meaning the least healing and 5 being excellent healing.

Secondary Outcomes

  • soft tissue thickness in millimeters.(4 months)
  • pain score on the visual analogue scale (VAS)(1 week)
  • Bone width and height measured in millimeters(4 months)

Investigators

Sponsor
Hams Hamed Abdelrahman
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Assistant lecturer

Alexandria University

Study Sites (1)

Loading locations...

Similar Trials