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Comparison of Er,Cr:YSGG and Diode Lasers In Second Stage Implant Surgery

Y

Yuzuncu Yıl University

Status

Completed

Conditions

Soft Tissue Bleeding
Postoperative Pain
Wound Heal

Treatments

Device: 2780 nm Er,Cr:YSGG Laser
Device: 940 nm Gallium Aluminum Arsenide Diode Laser

Study type

Interventional

Funder types

Other

Identifiers

NCT03819244
24112017-01

Details and patient eligibility

About

The study evaluates postoperative pain, intraoperative bleeding and wound healing after second stage implant surgery. Submerged implants were exposed with diode laser in Group 1 (n=20) and by using Er,Cr:YSGG laser in Group 2 (n=20).

Enrollment

40 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • subject has osseointegrated implants embedded under oral mucosa.
  • subject undergoes second-stage implant surgery.

Exclusion criteria

  • inadequate keratinized gingiva in the implant site.
  • localization of the implant site is not possible due to excessive thickness of the oral mucosa

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

Diode laser
Experimental group
Description:
Soft tissue incision with 940 nm Gallium Aluminum Arsenide diode laser, at implant recovery settings (2.5 W output power, average power: 1.25 W, pulse length : 1.00 ms, pulse interval: 1.00 ms) in second-stage implant surgery.
Treatment:
Device: 940 nm Gallium Aluminum Arsenide Diode Laser
Erbium laser
Experimental group
Description:
Soft tissue incision with 2780 nm Er,Cr:YSGG laser, at implant recovery settings (2.00 W power, 100 Hz, H mode, 10% water and 10% air) in second-stage implant surgery.
Treatment:
Device: 2780 nm Er,Cr:YSGG Laser

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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