Clinical Trials Directory

Trials / Completed

CompletedNCT02711501

Comparison of Post-operative Complications of Bone Augmentation at Anterior of Maxilla After Periosteal Releasing Incision With Two Techniques Diode Laser and Scalpel

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Tehran University of Medical Sciences · Academic / Other
Sex
All
Age
30 Years – 45 Years
Healthy volunteers
Not accepted

Summary

The aim of this study was to investigate if using lasers instead of scalpel for flap advancement in bone augmentation procedures would reduce post-operative swelling and pain.

Detailed description

Guided bone regeneration (GBR) is a well established method to augment excessive alveolar bone loss before and at the time of implant placement. Primary closure of soft tissue is a prerequisite for successful bone augmentation procedures. Adequate flap advancement is a key factor for tension free primary wound closure. The tension free flap is usually attained by incising the buccal flap using scalpels. However, this procedure, especially in cases with major flap advancement, results in increased patient morbidity after surgery. Swelling and hemorrhage during the first week after surgery have a negative effect on patient's quality of life. Currently, lasers are widely used as a tool for soft tissue management and diode laser appears to be an effective tool for incision and excision of the soft tissue. The major advantageous property of lasers is ablation of tissue together with effective hemostasis, minimal swelling and virtually no pain.

Conditions

Interventions

TypeNameDescription
PROCEDURELaser-assisted surgery.laser-assisted surgery
PROCEDUREconventional surgery by bladeconventional surgery

Timeline

Start date
2016-03-01
Primary completion
2016-04-01
Completion
2016-05-01
First posted
2016-03-17
Last updated
2016-09-13

Locations

3 sites across 1 country: Iran

Source: ClinicalTrials.gov record NCT02711501. Inclusion in this directory is not an endorsement.