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Radicular Cyst Enucleation Using Piezosurgery Versus Conventional Surgery

Clinical And Radiographic Outcomes Of Radicular Cyst Enucleation Using Piezosurgery Versus Conventional Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04244422
Enrollment
14
Registered
2020-01-28
Start date
2018-09-01
Completion date
2020-01-18
Last updated
2020-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

RADICULAR CYSTS

Brief summary

AIM: The study was intended to evaluate the effectiveness of piezosurgery in enucleation of radicular odontogenic cysts in comparison to the conventional technique from both the clinical and radiographic perspectives.

Detailed description

METHODS: Fourteen (8 females and 6 males) patients with age range of 30-55 years who had radicular cysts associated with non-vital teeth, were operated at the Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University. The patients were randomly divided into 2 groups;1) the study group (7 patients) in which cyst enucleation using piezosurgery was employed, 2) control group in which the cysts were removed using the conventional technique. The following parameters were assessed; postoperative pain, time of operation, hemorrhage control and field visibility, ease of operation, neurosensory evaluation and radiographic percentage of change in bone defect volume between preoperative and 3-months postoperative values.

Interventions

OTHERPIEZOSURGERY VERSUS CONVENTIONAL SURGERY

Piezosurgery: SATLEC ACTEON peizotome 2 (A company of ACTEON Group, France) was used. Conventional surgery with rotary instruments

Sponsors

Alexandria University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
31 Years to 52 Years
Healthy volunteers
Yes

Inclusion criteria

* 1\) Periapical cysts involving more than one tooth in close relation to the maxillary sinus, nasal cavity or inferior alveolar neurovascular bundle, * 2\) Intact labial/buccal cortical plate with no perforation.

Exclusion criteria

* 1\) Patients with systemic diseases contraindicating surgery * 2\) Cases in suspicion of malignancy

Design outcomes

Primary

MeasureTime frameDescription
Time of operation in minutesIntraoperativeTime from start of the incision to the last suture.
Hemorrhage control and ease of operation using a visual analogue scaleIntraoperativeTo assess the visibility of the field and ease of operation, a visual analogue scale was used. Each parameter constituted a horizontal 100 mm continuous line in which value of zero indicates minimum level of the assessed parameter and 100 indicates the maximum level. Each surgeon marked on the line then the score is determined by measuring in mms from the left end of the line to that marked point. (higher scores mean a better outcome)
Objective assessment of neurosensory function using a probe (to detect nerve injury after the surgeries)1 monthA probe was used to prick the patient's skin relevant to the area of operation to assess the neurosensory function in comparison to the contralateral side.If the patient states a difference in sensation between the side of operation and the normal side, it was assigned as Y and if there was no difference in sensation between the two sides, it was assigned as N.
Radiographic percentage of change in bone defect volume using cone beam computed tomography3 monthsThe change between preoperative and 3-months postoperative values of both groups were compared

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026