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Evaluation the effect of low level laser therapy in management of the complications after guided bone regeneration(GBR) surgeries.

Evaluation of the effect of using low level laser therapy in management of the complications of guided bone regeneration(GBR) surgeries in patients who need this surgery

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20221023056272N1
Enrollment
22
Registered
2023-04-29
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Post-operative complications of guided bone regeneration. Other specified complications of surgical and medical care, not elsewhere classified, initial encounter

Interventions

Intervention 1: Intervention group: Laser radiation: In the laser radiation group, immediately after the surgery for each patient, the surgical site will be irradiated with Diode laser with a waveleng

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients must be medically healthy Having healthy oral mucosa. Not having the history of implant failure at the surgical site or contraindications for implant placement Patients must be in need of bone grafting for placement of implant Cases, with maximum 0.5cc bone powder required for bone grafting, are going to be chosen The surgical field should be limited to 1 to 3 teeth Patients should not use removable prosthesis or similar items No history of medical conditions that might delay wound healing process such as: diabetes, smoking, and alcohol consumption.

Exclusion criteria

Exclusion criteria: Lack of Patient's cooperation Having photosensitivity Patients who have used antibiotics and corticosteroids for any reason in the last 2 weeks

Design outcomes

Primary

MeasureTime frame
The VAS(visual analog scale) number of pain intensity declared by patients. Timepoint: At 12, 24, 48, 72 hours after surgery. Method of measurement: based on VAS (visual analog scale).;The assigned number of the hemostasis status. Timepoint: On second day after surgery. Method of measurement: The number assigned to each hemostasis status is based on the following classification: 0 for the presence of bleeding in the wound margin/1 for the presence of fibrin in the wound margin/2 for the absence of fibrin in the wound margin.;Determining the degree of wound healing based on assigned numbers. Timepoint: On the seventh day after surgery. Method of measurement: Wound healing is graded as follows: 0 for complete wound healing / 1 for wound healing and the presence of a thin line of fibrinous membrane / 2 for wound healing and the presence of fibrin / 3 for incomplete wound closure and the presence of a gap/ 4 no wound healing (necrosis).;Determining the degree of inflammation based on two factors: 1) the degree of redness of the wound margin 2) presence or absence of extraoral swelling. Timepoint: On the second and seventh day after surgery. Method of measurement: To check the redness of the wound margin, the following grading is used: 0 for redness over 50% of the length of the wound margin / 1 for redness less than 50% of the length of the wound margin / 2 no redness.

Secondary

MeasureTime frame
The number and dose of painkillers taken by the patient. Timepoint: On seventh day after surgery. Method of measurement: After the surgery, the patient is given a table and asked to make notes in the table after receiving each painkiller. And the table is delivered on the seventh day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAsma Moghadasi

Ahvaz University of Medical Sciences

asma.moghadasi98@gmail.com+98 61 3333 5830

Outcome results

None listed

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