ClinicalTrials.Veeva

Menu

Low Intensity Pulsed Ultrasound Versus Low Level Laser Therapy Post Dental Implant

A

Ahram Canadian University

Status

Completed

Conditions

Surgical Dental Prostheses
Dental Implantation
Dental Implant

Treatments

Device: Low intensity pulsed ultrasound (LIPUS)
Device: low level diode laser therapy
Other: Standard Care

Study type

Interventional

Funder types

Other

Identifiers

NCT05938868
012/470001072023

Details and patient eligibility

About

The purpose of the study is to investigate the significance difference between low intensity pulsed ultrasound (LIPUS) versus low-level laser therapy (LLLT) on osseointegration, soft tissue healing, pain pressure threshold and oral health related quality of life in patients post dental implant surgery.

Enrollment

63 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Adult Patients.
  2. Both sexes will be contributed in the study.
  3. Non-smokers.
  4. Patients who needed dental implant in the maxillary or in the mandible.
  5. Bone height and width no less than Class III bone quality assessed clinically and radiologically.

Exclusion criteria

  1. Medically compromised patients as Uncontrolled diabetes mellitus.
  2. Patients indicated for bone graft at the implant site.
  3. Patients under chemotherapy or radiotherapy in facial region.
  4. Poor oral hygiene.
  5. Patients with any history of temporomandibular joint disorders.
  6. Patients with any other periodontal and oral surgeries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

63 participants in 3 patient groups

Group A (LIPUS group)
Experimental group
Description:
This group will include 17 patients who received Dental Implant Surgery. Patients will be treated with low intensity pulsed ultrasound in addition to standard care.
Treatment:
Other: Standard Care
Device: Low intensity pulsed ultrasound (LIPUS)
Group B (LLLT group)
Experimental group
Description:
This group will include 17 patients who received Dental Implant Surgery. The patients will be irradiated with low level diode laser therapy (GaAs) in addition to standard care.
Treatment:
Other: Standard Care
Device: low level diode laser therapy
Group C (Control group)
Active Comparator group
Description:
This group will include 17 patients who received Dental Implant Surgery. Patients will be treated with standard care only after surgery for 2 weeks.
Treatment:
Other: Standard Care

Trial contacts and locations

1

Loading...

Central trial contact

Mohamed M ElMeligie, Ph.d; Esraa S Elazab, MSc.

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems