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Clinical Trials/NCT04998292
NCT04998292UnknownNot Applicable

Piezo-surgical Implant Placement With Laser

Cairo University1 site in 1 country30 target enrollmentStarted: July 21, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
30
Locations
1
Primary Endpoint
Assessment of pain using visual analog scale

Study Overview

Brief Summary

Evaluation of the effect of laser with piezo-surgical device in dental implants

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 49 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Healthy subjects having good oral hygiene
  • History of bilateral extractions in the lower molar area not less than 6 months ago.

Exclusion Criteria

  • Patients with debilitating diseases or bad oral hygiene,
  • Patients with parafunctional habits and patients who are taking analgesics or with alcohol abuse.

Outcomes

Primary Outcomes

Assessment of pain using visual analog scale

Time Frame: 7 days after surgery

Assessment of pain

Time Frame: 2 hours after surgery

Secondary Outcomes

  • Swelling(3 days after surgery)
  • Swelling using swelling score system(7 days after surgery)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mahmoud Sedky

Principal investigator

Cairo University

Study Sites (1)

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