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Investigating the effect of diode laser with a wavelength of 840 nanometers on implant surgical complications

Investigating the effect of low-power diode laser with a wavelength of 840 nanometers on implant surgical complications of patients aged 18 to 60 years in Sari city in 2024

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221228056958N3
Enrollment
60
Registered
2024-11-17
Start date
2024-10-11
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Implant Surgery.

Interventions

Intervention 1: The implant used in the study will be Bone level with SLA level along with two-stage surgery (closing screw cover) along with covering the implant with gingiva. Brand implants (Dentis

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: People with systemic health (class 1 according to the ASA classification) cooperative good oral hygiene and absence of acute infection Patients with teeth indicated for extraction due to terminal periodontal disease, root fracture, or root resorption Patients who were willing to visit again. Patients should not have untreated periodontal disease.

Exclusion criteria

Exclusion criteria: Patients with compromised systemic conditions (ASA 2,3,4,5,6) Inadequate oral hygiene and presence of acute infection Patients without teeth indicated for extraction or unwilling for implant treatment Patients unwilling to visit again Patients with untreated periodontal disease Uncooperative

Design outcomes

Primary

MeasureTime frame
Swelling. Timepoint: Before surgery, 2, 4 and 7 days after surgery. Method of measurement: Swelling is evaluated with a measuring tape using the following signs: point A: from the tragus of the ear to the corner of the mouth and point B: from the lateral canthus of the eye to the corner of the mouth. Sizes are recorded in millimeters.;Mouth opening. Timepoint: Before surgery, 2, 4 and 7 days after surgery. Method of measurement: Mouth opening is evaluated by recording the distance between the upper and lower incisal teeth.;Pain. Timepoint: 2, 4 and 7 days after surgery. Method of measurement: Pain is evaluated by VAS method (0-10) 0 (no pain or discomfort), 1-4 (mild pain), 5-6 (moderate pain), and 7-10 (severe pain).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Najme Sadat Valed Saravi

Mazandaran University of Medical Sciences

n.valed@mazums.ac.ir+98 11 3304 4000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026