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Evaluation of the effect of laser on repair and pain caused by surgical crown lengtheningn

Evaluation of the effect of Diode Laser of 808 nm and 660 nm in tissue repair and pain due to surgical crown lengthening

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110109005570N12
Enrollment
20
Registered
2021-08-23
Start date
2021-07-06
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

surgical crown length.

Interventions

After surgical crown lengthening, in case group diode laser with a wavelength of 660 nm, 40 mW power, continuously, 30 seconds and 808nm wavelength, 200mw power, continuously, 25 second laser irradi

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 60 Years

Inclusion criteria

Inclusion criteria: Systemically healthy patients From 25 years to 60 years Patients who have at least two teeth with the need for surgical crown lengthening in different quadrants of the mouth and not adjacent to each other

Exclusion criteria

Exclusion criteria: Patients with a history of periodontal surgery in the past six months Uncontrolled systemic disease Long-term treatment with antibiotics or steroids poor hygiene low cooperation smoking habit General contraindications for laser therapy

Design outcomes

Primary

MeasureTime frame
Clinical signs of re-epithelialization. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0: there is a distance between the gingival margins, 3: the gingival margins are adjacent, 6: the gingival margin has an overlap.;Clinical signs of inflammation. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0: redness above 50% of the length of the incision or swelling is visible, 1: redness is seen below 50% 2: redness is not seen.;Clinical signs of haemostasis. Timepoint: third and seventh days after surgery. Method of measurement: Observational, 0. : Bleeding is seen, 1: Fibrin is seen, 2: There is no fibrin.

Secondary

MeasureTime frame
Pain at the surgical site. Timepoint: Surgery day, first day, third day. Seventh day after surgery. Method of measurement: visual analog scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParichehr Behfarnia

Esfahan University of Medical Sciences

dr.pbehfarnia@gmail.com+98 31 3792 5570

Outcome results

None listed

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