Clinical Trials Directory

Trials / Completed

CompletedNCT04518956

Shockwave Therapy Versus LIPUS on Mandibular Fracture Bone Healing

Comparative Study Between the Effect of Shockwave Therapy and Low-intensity Pulsed Ultrasound (LIPUS) on Bone Healing of Mandibular Fracture

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
21 (actual)
Sponsor
Hams Hamed Abdelrahman · Academic / Other
Sex
All
Age
20 Years – 40 Years
Healthy volunteers
Not accepted

Summary

compare between the effect of shockwave therapy and low-intensity pulsed ultrasound on healing process of fresh mandibular fractures

Detailed description

The mandible is the commonest facial bone to fracture. Mandibular fractures represent more than 74% of all maxillofacial fractures. To compare between the effect of shockwave therapy and low-intensity pulsed ultrasound on healing process of fresh mandibular fractures. A total of 21 patients; aged between 20-40 years, who have mandibular fracture were selected for this study from the outpatient clinic of the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University. In this study all patients were subjected to closed reduction and intermaxillary fixation. This will be followed by shockwave therapy in seven patients as a study group and by low-intensity pulsed ultrasound in seven patients as study group. Seven patients will receive neither and will constitute the control group.

Conditions

Interventions

TypeNameDescription
PROCEDUREinter maxillary fixation with shockwave therapyShockwave therapy device which give 1500-4000 pulses per session with or without anesthesia, and the treatment session takes approximately 5-10 minutes at the day after surgery.
PROCEDUREInter maxillary fixation and exposure to low intensity pulsedLow-intensity pulsed ultra sound was applied three times weekly for six weeks from the second day after surgery.
PROCEDUREInter maxillary fixationClosed reduction will be done. Intermaxillary fixation (IMF) will be secured after proper reduction of the fractured segments to assure proper occlusion using upper and lower arch bars or eyelet wires for six weeks.

Timeline

Start date
2016-12-18
Primary completion
2018-02-07
Completion
2018-06-23
First posted
2020-08-19
Last updated
2020-08-19

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04518956. Inclusion in this directory is not an endorsement.