Evaluation of the effect of 980 nm diode laser along with modified Wiedemann flap surgery on periodontal parameters

Evaluation of the effect of 980 nm diode laser along with modified Wiedemann flap surgery on periodontal parameters in patients with chronic periodontitis

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20231123060153N1

Enrollment

Registered

2024-06-08

Start date

2024-05-21

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

Chronic periodontitis disease.

Interventions

Intervention group: Patients receive surgical treatment without laser radiation in one jaw quadrant.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with chronic periodontitis with a pocket depth of more than 5 mm Having at least 20 teeth Systemically healthy people

Exclusion criteria

Exclusion criteria: Patients who are under any drug treatment that affects the periodontium Pregnant or lactating patients Patients who have used antibiotics continuously (one full week) during the last 3 months Patients who consume alcohol Patients who smoke and use tobacco Patients who have received periodontal treatment in the last 6 months The presence of orthodontic appliances or various types of prostheses in the treatment area Non-cooperation of the patient/emigration or death/non-observance of hygiene during the follow-up procedures Suffering from one of the diseases affecting the study process

Design outcomes

Primary

Measure	Time frame
PPD (pocket probing depth). Timepoint: Clinical parameters are recorded before surgery and 3 and 6 months after surgery for all sites. Method of measurement: Williams probe is used to measure clinical parameters.;CAL (clinical attachment loss). Timepoint: Before surgery, three months later, 6 months later. Method of measurement: It is measured by a williams probe.;BOP (bleeding on probing). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: By probing the area and checking the amount of bleeding.;GR (gingival recession). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: Using William's probe, we check the amount of gingival recession.;PI (plaque index). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: It is measured by a probe.	—

Measure

Time frame

PPD (pocket probing depth). Timepoint: Clinical parameters are recorded before surgery and 3 and 6 months after surgery for all sites. Method of measurement: Williams probe is used to measure clinical parameters.;CAL (clinical attachment loss). Timepoint: Before surgery, three months later, 6 months later. Method of measurement: It is measured by a williams probe.;BOP (bleeding on probing). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: By probing the area and checking the amount of bleeding.;GR (gingival recession). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: Using William's probe, we check the amount of gingival recession.;PI (plaque index). Timepoint: Before surgery, 3 months after, 6 months after. Method of measurement: It is measured by a probe.

—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir reza Ahmadinia

Gorgan University of Medical Sciences

ar.ahmadinia@gmail.com+98 17 3253 6270

Outcome results

None listed

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